Filed
Pursuant to Rule 424(b)(3)
Registration No. 333-269077
9,978,100,000
Shares of Common Stock Offered by Selling Stockholders
This
prospectus relates to the resale, from time to time, by the selling stockholders listed in this prospectus under the section “Selling
Stockholders,” of up to 9,978,100,000 shares of common stock, par value $.0001 per share, of Rennova Health, Inc., issuable
upon the exercise of Series B Warrants which we sold to the Selling Stockholders in private placements on March 21, 2017.
Our
common stock is traded on the OTC Pink under the symbol “RNVA.” The last reported sales price of our common stock on May
10, 2023 was $0.0001 per share. There were 29,934,322,257 shares of our common stock outstanding as of May 1, 2023.
The
Selling Stockholders may sell the shares of common stock being offered by this prospectus from time to time on terms to be determined
at the time of sale through ordinary brokerage transactions or through any other means described in this prospectus under “Plan
of Distribution.” The Selling Stockholders may sell the common stock at a fixed price of $0.00014 per share until our common
stock is quoted on the OTCQB or OTCQX marketplace, or listed on a national securities exchange. Thereafter, the prices at which the Selling
Stockholders may sell the shares will be determined by the prevailing market price for the shares or in negotiated transactions. We are
not selling any securities under this prospectus and we will not receive any proceeds from the sale of the shares by the Selling Stockholders.
However, we may receive proceeds from the cash exercise of the Series B Warrants which, if exercised in full in cash, would result in
gross proceeds of $898,029. See the section entitled “Use of Proceeds” on page 18 of this prospectus.
Investing
in our securities involves a high degree of risk. See “Risk Factors” beginning on page 3 of this prospectus for a
discussion of information that should be considered in connection with an investment in our securities.
Neither
the Securities and Exchange Commission nor any state securities commission has approved or disapproved of these securities or determined
if this prospectus is truthful or complete. Any representation to the contrary is a criminal offense.
___________
The
date of this prospectus is May 12, 2023
TABLE
OF CONTENTS
ABOUT
THIS PROSPECTUS
This
prospectus is part of a registration statement that we have filed with the Securities and Exchange Commission (the “SEC”
or the “Commission”). By using such registration statement, the Selling Stockholders may, from time to time, offer and sell
shares of our common stock pursuant to this prospectus. It is important for you to read and consider all of our information contained
in this prospectus before making any decision whether to invest in the common stock. You should also read and consider the information
contained in the documents that we have incorporated by reference as described in “Where You Can Find Additional Information,”
and “Incorporation of Certain Information by Reference” in this prospectus.
We
and the Selling Stockholders have not authorized anyone to give any information or to make any representations different from that which
is contained or incorporated by reference in this prospectus in connection with the offer made by this prospectus and, if given or made,
such information or representations must not be relied upon as having been authorized by Rennova Health, Inc. or any Selling Stockholder.
Neither the delivery of this prospectus nor any sale made hereunder and thereunder shall under any circumstances create an implication
that there has been no change in the affairs of Rennova Health, Inc. since the date hereof. You should assume that information contained
in this prospectus is accurate only as of the date on the front cover hereof. Our business, financial condition, results of operations
and prospects may have changed since that date. This prospectus does not constitute an offer or solicitation by anyone in any state in
which such offer or solicitation is not authorized or in which the person making such offer or solicitation is not qualified to do so
or to anyone to whom it is unlawful to make such offer or solicitation.
PROSPECTUS
SUMMARY
This
summary provides an overview of selected information contained elsewhere in this prospectus and does not contain all of the information
you should consider before investing in our securities. You should carefully read this prospectus and the registration statement of which
this prospectus is a part in their entirety before investing in our securities, including the information discussed under “Risk
Factors” and our financial statements and notes thereto that appear elsewhere in this prospectus or are incorporated by reference
in this prospectus. Unless otherwise indicated herein, the terms “we,” “our,” “us,” or the “Company”
refer to Rennova Health, Inc.
Rennova
Health, Inc. (“Rennova” or the “Company”) is a provider of healthcare services. We own one operating
hospital in Oneida, Tennessee, a hospital located in Jamestown, Tennessee that we plan to reopen and operate, and a rural health clinic in Kentucky. The Company’s operations consist
of only one business segment, Hospital Operations.
Hospital
Operations
We
believe that the acquisition or development of rural hospitals and related health-care services assets is a viable business strategy
and will create a stable revenue base from the provision of a needed service in rural America. These facilities deliver needed
healthcare services and employment to communities that would otherwise have to travel an hour or more to alternative locations.
Our
current operations began on August 8, 2017, following the receipt of the required licenses and regulatory approvals to open our
first hospital in Oneida, Tennessee. We had net revenues of approximately $13.0 million and approximately $3.2 million
during the years ended December 31, 2022 and 2021, respectively.
Scott
County Community Hospital (d/b/a Big South Fork Medical Center)
On
January 13, 2017, we acquired certain assets related to Scott County Community Hospital, based in Oneida, Tennessee (the “Oneida
Assets”). The Oneida Assets include a 52,000 square foot hospital building and 6,300 square foot professional building on approximately
4.3 acres. Scott County Community Hospital has 25 beds, a 24/7 emergency department and a laboratory that provides a range of diagnostic
services. Scott County Community Hospital closed in July 2016 in connection with the bankruptcy filing of its parent company, Pioneer
Health Services, Inc. We acquired the Oneida Assets out of bankruptcy for a purchase price of $1.0 million. The hospital, which has been
renamed Big South Fork Medical Center, became operational on August 8, 2017. The hospital became certified as a Critical Access Hospital in December 2021, retroactive to June 30, 2021.
Jamestown
Regional Medical Center
On
June 1, 2018, we acquired from Community Health Systems, Inc. certain assets related to an acute care hospital located in Jamestown,
Tennessee, referred to as Jamestown Regional Medical Center, for a purchase price of $0.7 million. The hospital is an 85-bed facility
of approximately 90,000 square feet on over eight acres of land, which offered a 24-hour emergency department with two trauma bays and
seven private exam rooms, inpatient and outpatient medical services and a progressive care unit which provided telemetry services. The
acquisition also included a separate physician practice known as Mountain View Physician Practice, Inc.
The
Company suspended operations at the hospital and physician practice in June 2019, as a result of the termination of the hospital’s
Medicare agreement and other factors. The Company is evaluating whether to reopen the facility as an acute care hospital or as another
type of healthcare facility. Jamestown is located 38 miles west of Big South Fork Medical Center.
Jellico
Medical Center and CarePlus Clinic
On
March 5, 2019, we acquired certain assets related to a 54-bed acute care hospital that offered comprehensive services located in Jellico,
Tennessee known as Jellico Community Hospital and an outpatient clinic located in Williamsburg, Kentucky known as the CarePlus Center.
The hospital and the clinic and their associated assets were acquired from Jellico Community Hospital, Inc. and CarePlus Rural Health
Clinic, LLC, respectively. On March 1, 2021, the Company closed Jellico Community Hospital, after the City of Jellico issued a 30-day
termination notice for the lease of the building.
The
CarePlus Clinic offers compassionate care in a modern, patient-friendly facility. The CarePlus Clinic is located 32 miles northwest of
our Big South Fork Medical Center.
Discontinued
Operations
Sale
of Health Technology Solutions, Inc. and Advanced Molecular Services Group, Inc.
On
June 25, 2021, the Company sold its subsidiaries, Health Technology Solutions, Inc. (“HTS”) and Advanced Molecular
Services Group, Inc. (“AMSG”), including their subsidiaries, to InnovaQor, Inc. (“InnovaQor”), formerly
known as VisualMED Clinical Solutions Corporation. HTS and AMSG held Rennova’s software and genetic testing interpretation
divisions. In consideration for the shares of HTS and AMSG and the elimination of intercompany debt among the Company and HTS and AMSG,
InnovaQor issued the Company 14,950 shares of its Series B-1 Non-Voting Convertible Preferred Stock (the “InnovaQor Series B-1
Preferred Stock”). The Company recorded a gain on the sale of HTS and AMSG of $11.3 million in the year ended December 31, 2021,
of which $9.1 million resulted from the value of the 14,950 shares of the InnovaQor Series B-1 Preferred Stock and $2.2 million
resulted from the transfer to InnovaQor of the net liabilities of HTS and AMSG. We
have reflected the financial results of HTS and AMSG prior to the sale, as well as the gain on sales, as discontinued operations
in our consolidated financial statements incorporated by reference herein.
EPIC
Reference Labs, Inc.
During
the third quarter of 2020, we made a decision to sell EPIC Reference Labs, Inc. (“EPIC”) and to discontinue several
other non-operating subsidiaries, and as a result, EPIC’s operations and the other non-operating subsidiaries’
liabilities have been included in discontinued operations in the consolidated financial statements incorporated by reference in this
prospectus. We were unable to find a buyer for EPIC and, therefore, have ceased all efforts to sell EPIC and closed down its
operations.
Outlook
Rural healthcare
facilities provide a much-needed service to their local communities. Furthermore, owning a number of facilities in the same
geographic location will create numerous efficiencies in management, purchasing and staffing and will enable the provision of additional,
specialized and more valuable services that are needed by rural communities but cannot be sustained by a standalone facilities. We remain
confident that this is a sustainable model we can continue to grow through acquisition and development.
In
the second quarter of 2022, we formed a subsidiary, Myrtle Recovery Centers, Inc., to pursue opportunities in the behavioral sector initially
in our core, rural markets. We intend to focus on leveraging our existing physical locations and corporate and regional infrastructure
to offer behavioral services including, but not limited to, substance abuse treatment. Services will be provided on either an inpatient,
residential basis or an outpatient basis. The Company is finalizing its plans for these initiatives, which are subject to many factors,
including licensure and the hiring of clinical and operational staff. The Company intends to initially offer substance abuse services
at its Big South Fork Medical Center campus. The Company expects the facility to be open and operating in the second quarter of 2023
although there is no assurance that the Company will proceed with its plans.
Impact
of the Pandemic
The
COVID-19 pandemic was declared a global pandemic by the World Health Organization on March 11, 2020. We continue to closely monitor
the COVID-19 pandemic and its impact on our operations and we have taken steps intended to minimize the risk to our employees and
patients. These steps have increased our costs and our net revenues have been significantly adversely affected. As noted in
Notes 1, 7 and 8 to the consolidated financial statements incorporated by reference in this prospectus, we have received
Paycheck Protection Program loans (“PPP Notes”) as well as Department of Health and Human Services (“HHS”)
Provider Relief Funds and employee retention credits from the federal government. If the COVID-19 pandemic continues for a further
extended period, we expect to incur significant losses and additional financial assistance may be required. Going forward, we are
unable to determine the extent to which the COVID-19 pandemic will continue to affect our business. Our ability to make estimates of
the effect of the COVID-19 pandemic on net revenues, expenses or changes in accounting judgments that have had or are reasonably
likely to have a material effect on our financial statements is currently limited. The nature and effect of the COVID-19 pandemic on
our balance sheet and results of operations will depend on the severity and length of the pandemic in our service areas; government
activities to mitigate the pandemic’s effect; regulatory changes in response to the pandemic, especially those affecting rural
hospitals; existing and potential government assistance that may be provided; and the requirements of Provider Relief Fund receipts,
including our ability to retain such funds as have been received.
The
COVID-19 pandemic and the steps taken by governments to seek to reduce its spread have severely impacted the economy and the health care
industry in particular. Hospitals have especially been affected. Small rural hospitals, such as ours, may be overwhelmed by patients
if conditions worsen in their local areas. Staffing costs, and concerns due to the potential exposure to infections, may increase, as
may the costs of needed medical supplies necessary to keep the hospitals open. Doctors and patients may defer elective procedures and
other health care services. Travel bans, social distancing and quarantines may limit access to our facilities. Business closings and
layoffs in our local areas may result in the loss of insurance and adversely affect demand for our services, as well as the ability of
patients and other payers to pay for services as rendered.
These developments
have had, and may continue to have, a material adverse effect on us and the operations of our hospitals.
Corporate
Information
Effective
November 2, 2015, the Company, a Delaware corporation, changed its name from “CollabRx, Inc.” to “Rennova Health, Inc.”
The Company was previously named Tegal Corporation until 2012 when it acquired a private company named CollabRx, Inc. and changed its
name to “CollabRx, Inc.” Tegal Corporation was formed in December 1989 to acquire the operations of the former Tegal Corporation,
a division of Motorola, Inc. Tegal’s predecessor company was founded in 1972 and was acquired by Motorola, Inc. in 1978. Tegal
completed its initial public offering in October 1995.
The
Company’s fiscal year-end is December 31.
Our
principal executive offices are located at 400 South Australian Avenue, Suite 800, West Palm Beach, Florida 33401 and our telephone number
is (561) 855-1626. Our website address is www.rennovahealth.com. The information contained on, or that can be accessed through, our website
is not part of this prospectus.
THE
OFFERING
Securities
Offered by the Selling Stockholders |
|
9,978,100,000
shares of our Common Stock |
|
|
|
Offering
Price per Share |
|
The
Selling Stockholders may sell all or a portion of the shares being offered by this prospectus at a fixed price of $0.00014
per share until our Common Stock is quoted on the OTCQB or OTCQX marketplace, or listed on a national securities exchange. Thereafter,
the prices at which the Selling Stockholders may sell the shares will be determined by the prevailing market price at the time of
sale or at negotiated prices. See “Plan of Distribution.” |
|
|
|
Use
of Proceeds |
|
We
will not receive any of the proceeds from the sale by the Selling Stockholders of the shares of Common Stock. However, we may receive
proceeds from the cash exercise of the Series B Warrants which, if exercised in full in cash, would result in gross proceeds of $898,029.
See “Use of Proceeds.” |
|
|
|
Stock
Symbol |
|
RNVA |
|
|
|
Risk
Factors |
|
Investing
in our securities involves a high degree of risk. See “Risk Factors” beginning on page 3 of this prospectus for a
discussion of information that should be considered in connection with an investment in our securities. |
RISK
FACTORS
Investing
in our securities involves a high degree of risk. You should carefully consider the following risk factors, as well as the other information
in this prospectus, including our financial statements and related notes, which are incorporated by reference in this prospectus, before
deciding whether to invest in our securities. Information in this prospectus may be amended, supplemented or superseded from time to
time by reports we file with the SEC in the future. The occurrence of any of the adverse developments described in the following risk
factors could materially and adversely harm our business, financial condition, results of operations or prospects. In that case, the
trading price of our securities could decline, and you may lose all or part of your investment.
Risks
Related to this Offering
Our
common stock is subject to substantial dilution by exercises of warrants and conversions or exercises of other securities into common
stock.
The
Company has outstanding options, warrants, convertible preferred stock and convertible debentures. Exercise of the options and warrants,
and conversions of the convertible preferred stock and debentures could result in substantial dilution of our common stock and a decline
in its market price. In addition, the terms of certain of the warrants, convertible preferred stock and convertible debentures issued
by us provide for reductions in the per share exercise prices of the warrants and the per share conversion prices of the debentures and
preferred stock (if applicable and subject to a floor in certain cases), in the event that we issue common stock or common stock equivalents
(as that term is defined in the agreements) at an effective exercise/conversion price that is less than the then exercise/conversion
prices of the outstanding warrants, preferred stock or debentures, as the case may be. These provisions, as well as the issuances of
debentures and preferred stock with conversion prices that vary based upon the price of our common stock on the date of conversion, have
resulted in significant dilution of our common stock and have given rise to reverse splits of our common stock.
The
following table presents the dilutive effect of our various potential common shares as of December 31, 2022:
| |
December 31, 2022 | |
Common shares outstanding | |
| 29,084,322,257 | |
Dilutive potential shares: | |
| | |
Stock options | |
| 26 | |
Warrants | |
| 511,333,351,090 | |
Convertible debt | |
| 28,777,833,333 | |
Convertible preferred stock | |
| 452,995,411,111 | |
Total dilutive potential common shares, including outstanding common stock | |
| 1,022,190,917,817 | |
Continued
conversions and exercises of the Company’s outstanding securities into common stock have further depressed the market price of
our common stock and have caused corresponding decreases of the exercise and conversion prices of much of the remaining convertible securities
due to their anti-dilution provisions.
The
sale of a substantial amount of our common stock, including resale of the shares of common stock issuable upon the exercise of the Warrants
held by the Selling Stockholders, in the public market could adversely affect the prevailing market price of our common stock.
Sales
of substantial amounts of shares of our common stock in the public market, or the perception that such sales might occur, could adversely
affect the market price of our common stock, and the market value of our other securities.
A
substantial number of shares of common stock are being offered by this prospectus, and we cannot predict if and when the Selling Stockholders
may sell such shares in the public markets. Furthermore, in the future, we may issue additional shares of common stock or other equity
or debt securities convertible into common stock in connection with a financing, acquisition, litigation settlement, employee arrangement,
or otherwise. Any such issuance could result in substantial dilution to our existing stockholders and could cause our stock price to
decline.
Risks
Related to the Company
The
Company’s operations have historically operated at a loss and with a cash deficiency. The Company has limited access to capital
and is dependent on its ability to secure the funding required to cover current losses and execute on its business plan until cash flow
break even. Unless we raise sufficient funds, we will not be able to execute our business model.
For
the years ended December 31, 2022 and 2021, we have relied on issuances of preferred stock, notes payable, loans from a
former member of our Board of Directors, and various federal government loan and grant programs to fund our operations. We did not
generate positive cash flow from operating activities for the years ended December 31, 2022 and 2021.
Cash
deficiencies may make retention of employees difficult. Unless this situation is corrected we may lose employees to the point where
it becomes difficult to operate, or we may fail to attract employees to positions necessary to implement our business model.
Losses
incurred to date have created a need for additional capital, often at short notice, required for the Company to remain in business.
If this trend were to continue and we are unable to raise sufficient capital to fund our operations through other sources, our business
will be adversely affected, and we may not be able to continue as a going concern (see Management’s Discussion and Analysis
of Financial Condition and Results of Operations, “Liquidity and Capital Resources”). There can be no assurances that
we will be able to raise sufficient funds on terms that are acceptable to us, or at all, to fund our operations under our current business
model.
The
holders of our Series M Convertible Preferred Stock have, in the aggregate, votes equal to 51% of the Company’s voting securities
and the holders of the Series M Convertible Preferred Stock have granted an irrevocable proxy to our Chief Executive Officer.
During
2020, the Company issued its Series M Convertible Preferred Stock (the “Series M Preferred Stock”). Regardless of the number
of shares of Series M Preferred Stock outstanding and so long as at least one share of Series M Preferred Stock is outstanding, the outstanding
shares of Series M Preferred Stock shall have the number of votes, in the aggregate, equal to 51% of all votes entitled to be voted at
any meeting of stockholders or action by written consent. This means that the holders of Series M Preferred Stock have sufficient votes,
by themselves, to approve or defeat any proposal voted on by the Company’s stockholders, unless there is a supermajority required
under applicable law or by agreement. Holders of our common stock, therefore, will not have any control on issues submitted to a vote
of stockholders.
Mr.
Diamantis owns all of the outstanding Series M Preferred Stock. On August 13, 2020, he granted an irrevocable proxy to vote the Series
M Preferred Stock to Seamus Lagan, the Chief Executive Officer, President and Interim Chief Financial Officer of the Company. As a result,
Mr. Lagan controls a majority of the voting securities of the Company.
Our holding company structure makes us dependent
on our subsidiaries for our cash flow and could serve to subordinate the rights of our shareholders to the rights of creditors of our
subsidiaries, in the event of an insolvency or liquidation of any such subsidiary.
Our Company acts as a holding company and, accordingly,
substantially all of our operations are conducted through our subsidiaries. Such subsidiaries are separate and distinct legal entities.
As a result, substantially all of our cash flow depends upon the earnings of our subsidiaries. In addition, we depend on the distribution
of earnings, loans or other payment by our subsidiaries. No subsidiary will have any obligation to provide our Company with funds for
our payment obligations. If there is an insolvency, liquidation or other reorganization of any of our subsidiaries, our shareholders
will have no right to proceed against their assets. Creditors of those subsidiaries will be entitled to payment in full for the sale
or other disposal of the assets of those subsidiaries before our Company, as a shareholder, would be entitled to receive any distribution
from that sale or disposal.
The
effects of the coronavirus pandemic have had, and may continue to have, a material adverse impact on our business,
results of operations and financial condition.
Demand
for services at our hospitals was substantially impacted by the COVID-19 pandemic. If the pandemic continues for a further
extended period, we would expect to incur lower net revenues and incur significant losses. Accordingly,
additional financial assistance may be required.
The
coronavirus pandemic and the steps taken by governments to seek to reduce its spread have severely impacted the economy and the health
care industry in particular. Hospitals have especially been affected. Small rural hospitals, such as ours, may be overwhelmed by patients
if conditions worsen in their local areas. Staffing costs, and concerns due to the potential exposure to infections, may increase, as
may the costs of needed medical supplies necessary to keep the hospitals open. Doctors and patients may defer elective procedures and
other health care services. Travel bans, social distancing and quarantines may limit access to our facilities. Business closings and
layoffs in our local areas may result in the loss of insurance and adversely affect demand for our services, as well as the ability of
patients and other payers to pay for services as rendered.
Although
our financial statements have been prepared on a going concern basis, we have accumulated significant losses and have negative cash flows
from operations that could adversely affect our ability to refinance existing indebtedness or raise additional capital to fund our operations
or limit our ability to react to changes in the economy or our industry which raise substantial doubt about our ability to continue as
a going concern.
If
we are unable to improve our liquidity position we may not be able to continue as a going concern. The consolidated financial statements
incorporated by reference in this prospectus do not include any adjustments that might result if we are unable to continue as
a going concern and, therefore, be required to realize our assets and discharge our liabilities other than in the normal course of business,
which could cause investors to suffer the loss of all or a substantial portion of their investment.
We
have accumulated significant losses and have negative cash flows from operations, and at December 31, 2022, we had a working
capital deficit and stockholders’ deficit of $42.9 million and $29.1 million, respectively. In addition, we
incurred a loss from continuing operations of $3.3 million and $5.3 million for the years ended December 31, 2022 and 2021,
respectively, and we used cash of $0.2 million and $8.9 million to fund our operations during 2022 and 2021, respectively. Our cash position ($0.5
million at December 31, 2022) is critically deficient, and payments for our operations are not being made in the ordinary
course of business. The continued losses and other related factors, including past due accounts payable and payroll taxes as well as
payment defaults of certain outstanding debentures and notes payable, as more fully discussed in Notes 1, 7 and 8 to the
consolidated financial statements incorporated by reference in this prospectus, raise substantial doubt about our ability to
continue as a going concern for the next 12 months.
The
Company’s core business plan is to own and operate rural hospitals and other related healthcare service facilities, which
is a specialized marketplace with a requirement for capable and knowledgeable management. The Company’s current financial condition
may make it difficult to attract and maintain adequate expertise in its management team to successfully operate the Company’s hospitals.
There
can be no assurance that we will be able to achieve our business plan, which is to acquire and operate clusters of rural hospitals and
related assets, raise any additional capital or secure the additional financing necessary to implement our current operating plan. Our
ability to continue as a going concern is dependent upon our ability to raise adequate capital to fund our operations and repay our outstanding
debentures and other past due obligations, fully align our operating costs, increase our net revenues and eventually gain profitable
operations. The consolidated financial statements incorporated by reference in this prospectus do not include any adjustments
that might be necessary if we are unable to continue as a going concern.
The Company sold several of its subsidiaries
to InnovaQor and has a current convertible preferred stock investment in and note receivable with InnovaQor. An inability to monetize
its convertible preferred stock investment and/or receive cash proceeds in connection with repayment of the note receivable could have
a material adverse effect on the Company.
In June 2021, the Company sold several of its
information technology related subsidiaries to InnovaQor for 14,950 shares of InnovaQor Series B-1 Preferred Stock. In addition, the
Company has provided loans/advances to InnovaQor to fund its working capital needs; such loans were restructured on December 31, 2022
into a note receivable in the amount of $1.5 million. The Company has provided additional funds to InnovaQor since December 31, 2022
and expects to continue to do so until InnovaQor raises third-party capital. Modest liquidity in InnovaQor’s common stock continues
to affect the prospects for monetization of the Company’s preferred stock investment. Also, any delay in InnovaQor’s ability
to raise third-party capital may affect the timing of repayment of the note receivable, the liquidity of its common stock and the need
for continued funding of InnovaQor by the Company. The Company and InnovaQor may seek to restructure the terms of the note receivable
in the future. All such factors could have a material adverse effect on the Company.
The InnovaQor Series B-1 Preferred Stock and the
note receivable represent a significant portion of the Company’s assets. There is no assurance that InnovaQor will be able to continue
as a going concern. If that were not to happen it would have a material adverse effect on the Company.
Our
results of operations may be adversely affected if the Patient Protection and Affordable Care Act (“ACA”) is repealed, replaced
or otherwise changed.
The
ACA has increased the number of people with health care insurance. It also has reduced Medicare and Medicaid reimbursements. Numerous
proposals continue to be discussed to repeal, amend or replace the law. We cannot predict whether any such repeal, amend or replace proposals,
or any parts of them, will become law and, if they do, what their substance or timing will be. There is uncertainty whether, when and
how the ACA may be changed, what alternative provisions, if any, will be enacted, the timing of enactment and implementation of any alternative
provisions and the impact of any alternative provisions on providers as well as other healthcare industry participants. Efforts to repeal
or change the ACA or implement other initiatives intended to reform healthcare delivery and financial systems may have an adverse effect
on our business and results of operations.
We
may have a limited ability to use some or all of our net operating loss carryforwards in the future.
Under
Section 382 of the Internal Revenue Code of 1986, as amended, substantial changes in our ownership may limit the amount of net operating
loss carryforwards that could be utilized annually in the future to offset our taxable income. Specifically, this limitation may arise
in the event of a cumulative change in ownership of the Company of more than 50% within a three-year period. Any such annual limitation
may significantly reduce the utilization of our net operating loss carryforwards before they expire. The Company has federal net operating
loss carryforwards totaling approximately $73.6 million generated since 2016. It also has various state net operating loss carryforwards
that begin to expire in 2032. Transactions that may occur in the future may trigger an ownership change pursuant to Section 382,
and prior transactions may be deemed to have triggered an ownership change pursuant to Section 382, the result of which could limit the
amount of net operating loss carryforwards that we can utilize annually to offset our taxable income, if any. The Company is reviewing
whether any prior transaction may have triggered a limitation under Section 382. Any such limitation, whether as a result of a prior
transaction or a transaction in the future, could have a material adverse effect on our future results of operations.
General
economic conditions.
Much
healthcare spending is discretionary and can be significantly impacted by economic downturns. When patients are experiencing personal
financial difficulties or have concerns about general economic conditions, they may choose to defer or forego elective surgeries and
other non-emergent procedures, which are generally more profitable lines of business for hospitals. In addition, employers may impose
or patients may select a high-deductible insurance plan or no insurance at all, which increases a hospital’s dependence on self-pay
revenue. Moreover, a greater number of uninsured patients may seek care in our emergency rooms.
We
are unable to quantify the specific impact of current or recent economic conditions on our business, however, we believe that the economic
conditions in the service areas in which our hospitals operate may have an adverse impact on our operations. Such impact can be expected
to continue to affect not only the healthcare decisions of our patients and potential patients but could also have an adverse impact
on the solvency of certain managed care providers and other counterparties to transactions with us.
Healthcare
plans have taken steps to control the utilization and reimbursement of healthcare services.
We
also face efforts by non-governmental third-party payers, including healthcare plans, to reduce utilization and reimbursement for healthcare
services.
The
healthcare industry has experienced a trend of consolidation among healthcare insurance plans and payers, resulting in fewer but larger
insurance plans with significant bargaining power to negotiate fee arrangements with healthcare providers. These healthcare plans, and
independent physician associations, may demand that providers accept discounted fee structures or assume all or a portion of the financial
risk associated with providing services to their members through capped payment arrangements. There are also an increasing number of
patients enrolling in consumer driven products and high deductible plans that involve greater patient cost-sharing.
The
increased consolidation among healthcare plans and payers increases the potential adverse impact of not being, or ceasing to be, a contracted
provider with any such insurer. The ACA includes provisions, including ones regarding the creation of healthcare exchanges, which may
encourage healthcare insurance plans to increase exclusive contracting.
We
expect continuing efforts to reduce reimbursements, to impose more stringent cost controls and to reduce utilization of services. These
efforts, including future changes in third-party payer rules, practices and policies or ceasing to be a contracted provider to many healthcare
plans, have had and may continue to have a material adverse effect on our business.
Some
of our operations are subject to federal and state laws prohibiting “kickbacks” and other laws designed to prohibit payments
for referrals and eliminate healthcare fraud.
Federal
and state anti-kickback and similar laws prohibit payment, or offers of payment, in exchange for referrals of products and services for
which reimbursement may be made by Medicare or other federal and state healthcare programs. Some state laws contain similar prohibitions
that apply without regard to the payer of reimbursement for the services. Under a federal statute, known as the “Stark Law”
or “self-referral” prohibition, physicians, subject to certain exceptions, are prohibited from referring their Medicare or
Medicaid program patients to providers with which the physicians or their immediate family members have a financial relationship, and
the providers are prohibited from billing for services rendered in violation of Stark Law referral prohibitions. Violations of the federal
Anti-Kickback Law and Stark Law may be punished by civil and criminal penalties, and/or exclusion from participation in federal health
care programs, including Medicare and Medicaid. States may impose similar penalties. The ACA significantly strengthened provisions of
the Federal False Claims Act and Anti-Kickback Law provisions, and other health care fraud provisions, leading to the possibility of
greatly increased qui tam suits by private citizen “relators” for perceived violations of these laws. There can be
no assurance that our activities will not come under the scrutiny of regulators and other government authorities or that our practices
will not be found to violate applicable laws, rules and regulations or prompt lawsuits by private citizen relators under federal or state
false claims laws. A qui tam lawsuit has been filed against the Company alleging violations of the False Claims Act. See “Legal
Proceedings”.
Federal
officials responsible for administering and enforcing the healthcare laws and regulations have made a priority of eliminating healthcare
fraud. For example, the ACA includes significant new fraud and abuse measures, including required disclosures of financial arrangements
with physician customers, lower thresholds for violations and increased potential penalties for violations. Federal funding available
for combating health care fraud and abuse generally has increased. While we seek to conduct our business in compliance with all applicable
laws and regulations, many of the laws and regulations applicable to our business, particularly those relating to billing and reimbursement
of services and those relating to relationships with physicians, hospitals and patients, contain language that has not been interpreted
by courts. We must rely on our interpretation of these laws and regulations based on the advice of our counsel and regulatory or law
enforcement authorities may not agree with our interpretation of these laws and regulations and may seek to enforce legal remedies or
penalties against us for violations.
From
time to time we may need to change our operations, particularly pricing or billing practices, in response to changing interpretations
of these laws and regulations, or regulatory or judicial determinations with respect to these laws and regulations. These occurrences,
regardless of their outcome, could damage our reputation and harm important business relationships that we have with healthcare providers,
payers and others. Furthermore, if a regulatory or judicial authority finds that we have not complied with applicable laws and regulations,
we would be required to refund amounts that were billed and collected in violation of such laws and regulations. In addition, we may
voluntarily refund amounts that were alleged to have been billed and collected in violation of applicable laws and regulations. In either
case, we could suffer civil and criminal damages, fines and penalties, exclusion from participation in governmental healthcare programs
and the loss of licenses, certificates and authorizations necessary to operate our business, as well as incur liabilities from third-party
claims, all of which could harm our operating results and financial condition.
Moreover,
regardless of the outcome, if we or physicians or other third parties with whom we do business are investigated by a regulatory or law
enforcement authority we could incur substantial costs, including legal fees, and our management may be required to divert a substantial
amount of time to an investigation.
To
enhance compliance with applicable health care laws, and mitigate potential liability in the event of noncompliance, regulatory authorities,
such as the OIG, have recommended the adoption and implementation of a comprehensive health care compliance program that generally contains
the elements of an effective compliance and ethics program described in Section 8B2.1 of the United States Sentencing Commission Guidelines
Manual, and for many years the OIG has made available a model compliance program. In addition, certain states require that health care
providers that engage in substantial business under the state Medicaid program have a compliance program that generally adheres to the
standards set forth in the Model Compliance Program. Also, under the ACA, HHS will require suppliers, such as the Company, to adopt,
as a condition of Medicare participation, compliance programs that meet a core set of requirements. While we have adopted, or are in
the process of adopting, healthcare compliance and ethics programs that generally incorporate the OIG’s recommendations, and training
our applicable employees in such compliance, having such a program can be no assurance that we will avoid any compliance issues.
We
conduct our business in a heavily regulated industry and changes in regulations or violations of regulations could, directly or indirectly,
harm our operating results and financial condition.
The
healthcare industry is highly regulated and there can be no assurance that the regulatory environment in which we operate will not change
significantly and adversely in the future. Areas of the regulatory environment that may affect our ability to conduct business include,
without limitation:
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federal
and state laws applicable to billing and claims payment; |
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federal
and state laws relating to licensure; |
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federal
and state anti-kickback laws; |
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federal
and state false claims laws; |
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federal
and state self-referral and financial inducement laws, including the federal physician anti-self-referral law, or the Stark Law; |
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coverage
and reimbursement levels by Medicare and other governmental payors and private insurers; |
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HIPAA,
along with the revisions to HIPAA as a result of the Health Information Technology for Economic and Clinical Health Act (“HITECH”),
and analogous state laws; |
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federal
and state regulation of privacy, security, electronic transactions and identity theft; |
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federal,
state and local laws governing the handling, transportation and disposal of medical and hazardous waste; |
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Occupational
Safety and Health Administration rules and regulations; |
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changes
to laws, regulations and rules as a result of the ACA; and |
|
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changes
to other federal, state and local laws, regulations and rules, including tax laws. |
These
laws and regulations are extremely complex and in many instances, there are no significant regulatory or judicial interpretations of
these laws and regulations. Any determination that we have violated these laws or regulations, or the public announcement that we are
being investigated for possible violations of these laws or regulations, could harm our operating results and financial condition. In
addition, a significant change in any of these laws or regulations may require us to change our business model in order to maintain compliance
with these laws or regulations, which could harm our operating results and financial condition.
Failure
to comply with complex federal and state laws and regulations related to submission of claims for services can result in significant
monetary damages and penalties and exclusion from the Medicare and Medicaid programs.
We
are subject to extensive federal and state laws and regulations relating to the submission of claims for payment for services, including
those that relate to coverage of our services under Medicare, Medicaid and other governmental health care programs, the amounts that
may be billed for our services and to whom claims for services may be submitted.
Our
failure to comply with applicable laws and regulations could result in our inability to receive payment for our services or result in
attempts by third-party payers, such as Medicare and Medicaid, to recover payments from us that have already been made. Submission of
claims in violation of certain statutory or regulatory requirements can result in penalties, including substantial civil money penalties
for each item or service billed to Medicare in violation of the legal requirement, and exclusion from participation in Medicare and Medicaid.
Government authorities may also assert that violations of laws and regulations related to submission or causing the submission of claims
violate the federal False Claims Act (“FCA”) or other laws related to fraud and abuse, including submission of claims for
services that were not medically necessary. Violations of the FCA could result in enormous economic liability. The FCA provides that
all damages are trebled. For example, we could be subject to FCA liability if it was determined that the services we provided were not
medically necessary and not reimbursable, particularly if it were asserted that we contributed to the physician’s referrals of
unnecessary services to us. It is also possible that the government could attempt to hold us liable under fraud and abuse laws for improper
claims submitted by an entity for services that we performed if we were found to have knowingly participated in the arrangement that
resulted in submission of the improper claims.
Our
facilities are subject to potential claims for professional liability, including existing or potential claims based on the acts or omissions
of third parties, which claims may not be covered by insurance.
Our
facilities are subject to potential claims for professional liability (medical malpractice) in connection with their operations, as well
as potentially acquired or discontinued operations. To cover such claims, professional malpractice liability insurance and general liability
insurance are maintained in amounts believed to be sufficient for operations, although some claims may exceed the scope or amount of
the coverage in effect. The assertion of a significant number of claims, either within a self-insured retention (deductible) or individually
or in the aggregate in excess of available insurance, could have a material adverse effect on our results of operations or financial
condition. Premiums for professional liability insurance have historically been volatile and we cannot assure you that professional liability
insurance will continue to be available on terms acceptable to us, if at all. The operations of hospitals also depend on the professional
services of physicians and other trained healthcare providers and technicians in the conduct of their respective operations, including
independent laboratories and physicians rendering diagnostic and medical services. There can be no assurance that any legal action stemming
from the act or omission of a third-party provider of healthcare services would not be brought against one of our hospitals, resulting
in significant legal expenses in order to defend against such legal action or to obtain a financial contribution from the third party
whose acts or omissions occasioned the legal action.
Our
success depends on our ability to attract and retain qualified healthcare professionals. A shortage of qualified healthcare professionals
could weaken our ability to deliver healthcare services.
Our
operations are dependent on the efforts, ability and experience of healthcare professionals, such as physicians, nurses, therapists,
pharmacists and lab technicians. Each facility’s success has been, and will continue to be, influenced by its ability to attract
and retain these skilled employees. A shortage of healthcare professionals, the loss of some or all of its key employees or the inability
to attract or retain sufficient numbers of qualified healthcare professionals could cause the operating performance of one or more of
our facilities to decline.
A
significant portion of our net revenues is dependent on Medicare and Medicaid payments and possible reductions in Medicare or Medicaid
payments or the implementation of other measures to reduce reimbursements may reduce our revenues.
A
significant portion of our net revenues is derived from the Medicare and Medicaid programs, which are highly regulated and subject to
frequent and substantial changes. Previous legislative changes have resulted in, and future legislative changes may result in, limitations
on and reduced levels of payment and reimbursement for a substantial portion of hospital procedures and costs.
Future
healthcare legislation or other changes in the administration or interpretation of governmental healthcare programs may have a material
adverse effect on our consolidated business, financial condition, results of operations or prospects.
Failure
to timely or accurately bill for our services could have a material adverse effect on our business.
Billing
for medical services is extremely complicated and is subject to extensive and non-uniform rules and administrative requirements. Depending
on the billing arrangement and applicable law, we bill various payers, such as patients, insurance companies, Medicare, Medicaid, physicians,
hospitals and employer groups. Changes in laws and regulations could increase the complexity and cost of our billing process. Additionally,
auditing for compliance with applicable laws and regulations as well as internal compliance policies and procedures adds further cost
and complexity to the billing process.
Missing,
incomplete, or incorrect information adds complexity to and slows the billing process, creates backlogs of unbilled services,
and generally increases the aging of accounts receivable and bad debt expense. Failure to timely or correctly bill may lead to our not
being reimbursed for our services or an increase in the aging of our accounts receivable, which could adversely affect our results of
operations and cash flows. Failure to comply with applicable laws relating to billing or even having to pay back amounts incorrectly
billed and collected could lead to various penalties, including: (1) exclusion from participation in CMS and other government programs;
(2) asset forfeitures; (3) civil and criminal fines and penalties; and (4) the loss of various licenses, certificates and authorizations
necessary to operate our business, any of which could have a material adverse effect on our results of operations or cash flows.
There
have been times when our accounts receivable have increased at a greater rate than revenue growth and, therefore, have adversely affected
our cash flows from operations. We have taken steps to implement systems and processing changes intended to improve billing procedures
and related collection results. However, we cannot assure that our ongoing assessment of accounts receivable will not result in the need
for additional provisions. Such additional provisions, if implemented, could have a material adverse effect on our operating results.
Our
operations may be adversely impacted by the effects of extreme weather conditions, natural disasters such as hurricanes and earthquakes,
hostilities or acts of terrorism and other criminal activities.
Our
operations are always subject to adverse impacts resulting from extreme weather conditions, natural disasters, hostilities or acts of
terrorism or other criminal activities. Such events may result in a temporary decline in the number of patients who seek our services
or in our employees’ ability to perform their job duties. In addition, such events may temporarily interrupt our ability to provide
our services. The occurrence of any such event and/or a disruption of our operations as a result may adversely affect our results of
operations.
Increased
competition, including price competition, could have a material adverse impact on our net revenues and profitability.
We
operate in a business that is characterized by intense competition. Our major competitors include large national hospitals that possess
greater name recognition, larger customer bases, and significantly greater financial resources and employ substantially more personnel
than we do. Many of our competitors have long established relationships. Although our hospitals operate in communities where they are
currently the only general acute care hospital, they face substantial competition from other hospitals in their respective regions.
Although these competing hospitals may be many miles away, patients in these markets may travel to these competing hospitals
as a result of local physician referrals, managed care plan incentives or personal choices. We cannot assure you that we will be able
to compete successfully with such entities in the future.
The
healthcare business is intensely competitive both in terms of price and service. Pricing of services is often one of the most significant
factors used by patients, health care providers and third-party payers in selecting a provider. As a result of the healthcare industry
undergoing significant consolidation, larger providers are able to increase cost efficiencies. This consolidation results in greater
price competition. We may be unable to increase cost efficiencies sufficiently, if at all, and as a result, our net earnings and cash
flows could be negatively impacted by such price competition. We may also face competition from companies that do not comply with existing
laws or regulations or otherwise disregard compliance standards in the industry. Additionally, we may also face changes in fee schedules,
competitive bidding for services or other actions or pressures reducing payment schedules as a result of increased or additional competition.
Additional competition, including price competition, could have a material adverse impact on our net revenues and profitability.
Continued
supply chain shortages could increase our costs of operations or adversely affect our results of operations.
Shortages,
delays, increased costs, and governmental restrictions arising from the COVID-19 pandemic or arising out of increased demand as the pandemic
wanes have disrupted and may continue to disrupt the ability of our facilities to procure items used in their operations. A severe inability
to obtain such items or substantially increased costs for the items could have an adverse effect on our results of operations if we are
unable to pass such costs along to patients.
Sustained
inflation could increase our costs of operations.
The
healthcare industry is very labor intensive and salaries and benefits are subject to inflationary pressures, as are supply and other
costs. In particular, like others in the healthcare industry, we continue to experience a shortage of nurses and other clinical
staff and support personnel, which has been exacerbated by the COVID-19 pandemic. We are treating patients with COVID-19 in our
facilities and, in some areas, the increased demand for care is putting a strain on our resources and staff, which has required us
to utilize higher-cost temporary labor and pay premiums above standard compensation for essential workers. The length and extent of
the disruptions caused by the COVID-19 pandemic are currently unknown; however, we expect such disruptions to continue. This
staffing shortage may require us to further enhance wages and benefits to recruit and retain nurses and other clinical staff and
support personnel or require us to hire expensive temporary personnel. Furthermore, we are unable to predict whether recent
inflationary spikes, which were initially thought to be transitory and due to pandemic recovery related demand, labor
shortages in selected markets, and supply chain issues will continue for an extended period of time. Substantially increased
costs of personnel, goods, and services could have an adverse effect on our results of operations if we are unable to pass such
costs along to patients. The concentration of our patients in persons for whom the cost of treatment is paid for under government
programs could substantially limit our ability to pass through such costs.
Failure
to maintain the security of patient-related information or compliance with security requirements could damage the Company’s reputation
with patients and cause it to incur substantial additional costs and to become subject to litigation.
Pursuant
to HIPAA and certain similar state laws, we must comply with comprehensive privacy and security standards with respect to the use and
disclosure of protected health information. Under the HITECH amendments to HIPAA, HIPAA was expanded to require certain data breach notifications,
to extend certain HIPAA privacy and security standards directly to business associates, to heighten penalties for noncompliance and to
enhance enforcement efforts. If the Company does not comply with existing or new laws and regulations relating to protecting the privacy
and security of personal or health information, it could be subject to monetary fines, civil penalties or criminal sanctions.
The
Company receives certain personal and financial information about its patients. In addition, the Company depends upon the secure transmission
of confidential information over public networks, including information permitting cashless payments. While we take reasonable and prudent
steps to protect this information, a compromise in the Company’s security systems that results in patient personal information
being obtained by unauthorized persons or the Company’s failure to comply with security requirements for financial transactions
could adversely affect the Company’s reputation with its customers and others, as well as the Company’s results of operations,
financial condition and liquidity. It could also result in litigation against the Company or the imposition of penalties.
Failure
of the Company to comply with emerging electronic transmission standards could adversely affect our business.
The
failure of our IT systems to keep pace with technological advances may significantly reduce our revenues or increase our expenses. Public
and private initiatives to create healthcare information technology (“HCIT”) standards and to mandate standardized clinical
coding systems for the electronic exchange of clinical information could require costly modifications to our existing HCIT systems. While
we do not expect HCIT standards to be adopted or implemented without adequate time to comply, if we fail to adopt or delay in implementing
HCIT standards, we could lose customers and business opportunities.
Compliance
with the HIPAA security regulations and privacy regulations may increase the Company’s costs.
The
HIPAA privacy and security regulations, including the expanded requirements under HITECH, establish comprehensive federal standards with
respect to the use and disclosure of protected health information by health plans, healthcare providers and healthcare clearinghouses,
in addition to setting standards to protect the confidentiality, integrity and security of protected health information. The regulations
establish a complex regulatory framework on a variety of subjects, including:
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● |
the
circumstances under which the use and disclosure of protected health information are permitted or required without a specific authorization
by the patient, including but not limited to treatment purposes, activities to obtain payments for the Company’s services,
and its healthcare operations activities; |
|
● |
a
patient’s rights to access, amend and receive an accounting of certain disclosures of protected health information; |
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● |
the
content of notices of privacy practices for protected health information; |
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● |
administrative,
technical and physical safeguards required of entities that use or receive protected health information; and |
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the
protection of computing systems maintaining Electronic Personal Health Information (“ePHI”). |
The
Company has implemented policies and procedures related to compliance with the HIPAA privacy and security regulations, as required by
law. The privacy and security regulations establish a “floor” and do not supersede state laws that are more stringent. Therefore,
the Company is required to comply with both federal privacy and security regulations and varying state privacy and security laws. In
addition, for healthcare data transfers from other countries relating to citizens of those countries, the Company may also be required
to comply with the laws of those other countries. The federal privacy regulations restrict the Company’s ability to use or disclose
patient identifiable data, without patient authorization, for purposes other than payment, treatment or healthcare operations (as defined
by HIPAA), except for disclosures for various public policy purposes and other permitted purposes outlined in the privacy regulations.
HIPAA, as amended by HITECH, provides for significant fines and other penalties for wrongful use or disclosure of protected health information
in violation of the privacy and security regulations, including potential civil and criminal fines and penalties. Due to the enactment
of HITECH and an increase in the amount of monetary financial penalties, government enforcement has also increased. It is not possible
to predict what the extent of the impact on business will be, other than heightened scrutiny and emphasis on compliance. If the Company
does not comply with existing or new laws and regulations related to protecting the privacy and security of health information it could
be subject to significant monetary fines, civil penalties or criminal sanctions. In addition, other federal and state laws that protect
the privacy and security of patient information may be subject to enforcement and interpretations by various governmental authorities
and courts resulting in complex compliance issues. For example, the Company could incur damages under state laws pursuant to an action
brought by a private party for the wrongful use or disclosure of confidential health information or other private personal information.
Health
care reform and related programs (e.g. Health Insurance Exchanges), changes in government payment and reimbursement systems, or changes
in payer mix, including an increase in capitated reimbursement mechanisms and evolving delivery models, could have a material adverse
impact on the Company’s net revenues, profitability and cash flow.
Our
services are billed to private patients, Medicare, Medicaid, commercial clients, managed care organizations (“MCOs”) and
third-party insurance companies. Bills may be sent to different payers depending on the medical insurance benefits of a particular patient.
Increases in the percentage of services billed to government and managed care payers could have an adverse impact on the Company’s
net revenues.
A
portion of the third-party insurance fee-for-service revenues are collectible from patients in the form of deductibles, copayments and
coinsurance. As patient cost-sharing increases, collectability may be impacted.
In
addition, Medicare and Medicaid and private insurers have increased their efforts to control the cost, utilization and delivery of health
care services. Measures to regulate health care delivery have resulted in reduced prices, added costs and decreased utilization as well
as increased complexity and new regulatory and administrative requirements. Changes to, or repeal of, the ACA, the health care reform
legislation passed in 2010, also may continue to affect coverage, reimbursement and utilization of services, as well as administrative
requirements, in ways that are currently unpredictable.
The
Company expects efforts to impose reduced reimbursement, more stringent payment policies and utilization and cost controls by government
and other payers to continue. If the Company cannot offset additional reductions in the payments it receives for its services by reducing
costs, increasing the number of patients treated and/or introducing new procedures, it could have a material adverse impact on the Company’s
net revenues, profitability and cash flows.
As
an employer, health care reform legislation also contains numerous regulations that will require the Company to implement significant
process and record keeping changes to be in compliance. These changes increase the cost of providing healthcare coverage to employees
and their families. Given the limited release of regulations to guide compliance, as well as potential changes to or repeal of the ACA,
the exact impact to employers including the Company is uncertain.
Adverse
results in material litigation matters or governmental inquiries could have a material adverse effect upon the Company’s business
and financial condition.
The
Company may become subject in the ordinary course of business to material legal action related to, among other things, professional liability,
contracts and employee-related matters, as well as inquiries and requests for information from governmental agencies and bodies and Medicare
or Medicaid payors requesting comment and/or information on allegations of billing irregularities, billing and pricing arrangements,
privacy practices and other matters that are brought to their attention through billing audits or third parties. The healthcare industry
is subject to substantial Federal and state government regulation and audit. Legal actions could result in substantial monetary damages
as well as damage to the Company’s reputation with customers, which could have a material adverse effect upon its business.
As
a company with limited capital and human resources, we anticipate that more of management’s time and attention will be diverted
from our business to ensure compliance with regulatory requirements than would be the case with a company that has well established controls
and procedures. This diversion of management’s time and attention may have a material adverse effect on our business, financial
condition and results of operations.
In
the event we identify significant deficiencies or material weaknesses in our internal control over financial reporting that we cannot
remediate in a timely manner, or if we are unable to receive a positive attestation from our independent registered public accounting
firm with respect to our internal control over financial reporting when we are required to do so, investors and others may lose confidence
in the reliability of our financial statements. If this occurs, the trading price of our common stock, if any, and ability to obtain
any necessary equity or debt financing could suffer. Presently, our auditors are not required to audit internal controls over financial
reporting. However, if in the future such a requirement arises, and in the event that our independent registered public accounting firm
is unable to rely on our internal control over financial reporting in connection with its audit of our financial statements, and in the
further event that it is unable to devise alternative procedures in order to satisfy itself as to the material accuracy of our financial
statements and related disclosures, we may be unable to file our periodic reports with the SEC. This would likely have an adverse effect
on the trading price of our common stock, if any, and our ability to secure any necessary additional financing, and could result in the
delisting of our common stock. In such event, the liquidity of our common stock would be severely limited and the market price of our
common stock would likely decline significantly.
An
inability to attract and retain experienced and qualified personnel could adversely affect the Company’s business.
The
loss of key management personnel or the inability to attract and retain experienced and qualified employees by the Company could adversely
affect the business. The success of the Company is dependent in part on the efforts of key members of its management team.
Failure
in the Company’s information technology systems or delays or failures in the development and implementation of updates or enhancements
to those systems could significantly delay billing and otherwise disrupt the Company’s operations or patient relationships.
The
Company’s business and patient relationships depend, in part, on the continued performance of its information technology systems.
Despite network security measures and other precautions, the Company’s information technology systems are potentially vulnerable
to physical or electronic break-ins, computer viruses and similar disruptions. Sustained system failures or interruption of the Company’s
systems in one or more of its operations could disrupt the Company’s ability to conduct its business. Breaches with respect to
protected health information could result in violations of HIPAA and analogous state laws, and risk the imposition of significant fines
and penalties. Failure of the Company’s information technology systems could adversely affect the Company’s business, profitability
and financial condition.
Increasing
health insurance premiums and co-payments or high deductible health plans may cause individuals to forgo health insurance and avoid medical
attention, either of which may reduce demand for our products and services.
Health
insurance premiums, co-payments and deductibles have generally increased in recent years. These increases may cause individuals to forgo
health insurance, as well as medical attention. This behavior may reduce demand for services at our hospitals.
Our
business has substantial indebtedness; the majority of our debt instruments are in payment default and contain restrictive
covenants which may affect our operational and financial flexibility.
We
currently have, and will likely continue to have, a substantial amount of indebtedness. Our indebtedness could, among other things,
make it more difficult for us to satisfy our debt and other obligations, require us to use a large portion of our cash flow from
operations to repay and service our debt or otherwise create liquidity problems, limit our flexibility to adjust to market
conditions and place us at a competitive disadvantage. Restrictive covenants in the agreements governing our indebtedness may
adversely affect us. As of December 31, 2022, we had total debt outstanding of approximately $14.5 million, all of
which is short term and the majority of which is past due. As a result of non-payments of debt, included in
outstanding debentures at both December 31, 2022 and 2021, were default payment penalties of $1.9 million and we have incurred
penalty interest on outstanding debentures and notes payable of approximately $1.8 million and $2.6 million during the years ended
December 31, 2022 and 2021, respectively.
Our
ability to meet our obligations depends on our future performance and capital raising activities, which will be affected by financial,
business, economic and other factors, many of which are beyond our control. If our cash flow and capital resources prove inadequate to
allow us to pay the principal and interest on our debt and meet our other obligations, we could face substantial liquidity problems
and might be required to dispose of material assets or operations, restructure or refinance our debt, which we may be unable to do on
acceptable terms, and forego attractive business opportunities. In addition, the terms of our existing or future debt agreements may
restrict us from pursuing any of these alternatives.
Failure
to achieve and maintain an effective system of internal control over financial reporting may result in our not being able to accurately
report our financial results. As a result, current and potential shareholders could lose confidence in our financial reporting, which
would harm our business and the trading price of our common stock.
Our
management has determined that as of December 31, 2022, we did not maintain effective internal control over financial reporting
based on criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission (“COSO”) in Internal
Control-Integrated Framework as a result of material weaknesses in our internal control over financial reporting. A material weakness
is a deficiency, or a combination of deficiencies, in internal control over financial reporting such that there is a reasonable possibility
that a material misstatement of the Company’s annual or interim financial statements will not be prevented or detected on a timely
basis. If the results of our remediation efforts regarding our material weaknesses are not successful, or if additional material weaknesses
or significant deficiencies are identified in our internal control over financial reporting, our management will be unable to report
favorably as to the effectiveness of our internal control over financial reporting and/or our disclosure controls and procedures, and
we could be required to further implement expensive and time-consuming remedial measures and potentially lose investor confidence in
the accuracy and completeness of our financial reports, which could have an adverse effect on our stock price and potentially subject
us to litigation.
Provisions
of Delaware law and our organizational documents may discourage takeovers and business combinations that our stockholders may consider
in their best interests, which could negatively affect our stock price.
Provisions
of Delaware law and our certificate of incorporation and bylaws may have the effect of delaying or preventing a change in control of
the Company or deterring tender offers for our common stock that other stockholders may consider in their best interests.
Our
certificate of incorporation authorizes us to issue up to 5,000,000 shares of preferred stock in one or more different series with terms
to be fixed by our Board of Directors. Stockholder approval is not necessary to issue preferred stock in this manner. Issuance of these
shares of preferred stock could have the effect of making it more difficult and more expensive for a person or group to acquire control
of us, and could effectively be used as an anti-takeover device.
Our
bylaws provide for an advance notice procedure for stockholders to nominate director candidates for election or to bring business before
an annual meeting of stockholders, including proposed nominations of persons for election to our Board of Directors, and require that
special meetings of stockholders be called only by our chairman of the board, chief executive officer, president or the board pursuant
to a resolution adopted by a majority of the board.
The
anti-takeover provisions of Delaware law and provisions in our organizational documents may prevent our stockholders from receiving the
benefit from any premium to the market price of our common stock offered by a bidder in a takeover context. Even in the absence of a
takeover attempt, the existence of these provisions may adversely affect the prevailing market price of our common stock if they are
viewed as discouraging takeover attempts in the future.
As
a public company, we incur significant administrative workload and expenses.
As
a public company, we must comply with various laws, regulations and requirements, including certain provisions of the Sarbanes-Oxley
Act of 2002, as well as rules implemented by the SEC. Complying with these statutes, regulations and requirements, including our public
company reporting requirements, continues to occupy a significant amount of the time of our Board of Directors and management and involves
significant accounting, legal and other expenses. We may need to hire additional accounting personnel to handle these responsibilities,
which will increase our operating costs. Furthermore, these laws, regulations and requirements could make it more difficult or more costly
for us to obtain certain types of insurance. The impact of these requirements
could also make it more difficult for us to attract and retain qualified persons to serve on our Board of Directors, our board committees
or as executive officers.
New
laws and regulations as well as changes to existing laws and regulations affecting public companies, including the provisions of the
Sarbanes-Oxley Act of 2002 and rules adopted by the SEC, would likely result in increased costs to us as we respond to their requirements.
We are investing resources to comply with evolving laws and regulations, and this investment may result in increased general and administrative
expenses and a diversion of management’s time and attention from revenue-generating activities to compliance activities.
We
do not intend to pay cash dividends on our common stock in the foreseeable future.
We
have never declared or paid cash dividends on our common stock and certain of our financing agreements, while outstanding, prohibit us
from declaring or paying cash dividends without approval, which may not be granted. In addition, we anticipate that we will retain our
earnings, if any, for future growth and therefore do not anticipate paying any cash dividends in the foreseeable future. The terms of
certain series of our Preferred Stock also preclude the payment of cash dividends on our common stock unless dividends are paid on such
Preferred Stock. Accordingly, our stockholders will not realize a return on their investment unless the trading price of our common stock
appreciates, which is uncertain and unpredictable.
We
have used our convertible preferred stock for the exchange/repayment of debt and to raise capital. Going forward, we may use our
stock to pay, to a large extent, for future acquisitions or we may continue to use our stock for the exchange/repayment of debt and
to raise capital, which has been and would continue to be dilutive to investors.
In
the past we have used our convertible preferred stock for the exchange/repayment of debt and to raise capital, which as a result
of the conversions of the preferred stock into a variable number of shares of our common stock, has resulted in significant dilution
of our common stock. Going forward, we may choose to use additional preferred or common stock to pay, to a large extent, for future acquisitions
or for additional exchanges/repayments of debt and to raise capital, and believe that doing so will enable us to retain
a greater percentage of our cash flows to fund operations and to obtain cash to fund our operations. Price fluctuations
in our stock might negatively impact our ability to effectively use our stock to pay for acquisitions, or could cause us to offer stock
as consideration for acquisitions on terms that are not favorable to us and our stockholders. If we issued shares of our convertible
preferred stock or our common stock in lieu of cash as consideration for acquisitions or in exchange/repayment of debt or to raise capital
under unfavorable circumstances, it may result in significant dilution to investors.
Our
operations are dependent on the local economies and the surrounding areas in which they operate and are concentrated in Tennessee.
A significant deterioration in those economies could cause a material adverse effect on our hospitals’ businesses.
Each
rural hospital operation is dependent upon the local economy where it is located. A significant deterioration in that economy would negatively
impact the demand for the facility’s services, as well as the ability of patients and other payers to pay for service as
rendered.
Our
revenues are particularly sensitive to regulatory and economic changes in the State of Tennessee. Any change in the current demographic,
economic, competitive or regulatory conditions in the state could have an adverse effect on our business, financial condition or results
of operations. Changes to the Medicaid program or other health care laws or regulations in that state could also have an adverse effect.
CAUTIONARY
STATEMENT CONCERNING FORWARD-LOOKING STATEMENTS
This
prospectus and those documents incorporated by reference in this prospectus contain forward-looking statements. Statements contained
in this prospectus that refer to the Company’s estimated or anticipated future results are forward-looking statements that reflect
current perspectives of existing trends and information as of the date of this prospectus. Forward-looking statements generally will
be accompanied by words such as “anticipate,” “believe,” “plan,” “could,” “should,”
“estimate,” “expect,” “forecast,” “outlook,” “guidance,” “intend,”
“may,” “might,” “will,” “possible,” “potential,” “predict,” “project,”
or other similar words, phrases or expressions. Such forward-looking statements include statements about the Company’s plans, objectives,
expectations and intentions. It is important to note that the Company’s goals and expectations are not predictions of actual performance.
Actual results may differ materially from the Company’s current expectations depending upon a number of factors affecting the Company’s
business. These risks and uncertainties include those set forth under “Risk Factors” beginning on page 3, as well
as, among others, business effects, including the effects of industry, economic or political conditions outside of the Company’s
control; the inherent uncertainty associated with financial projections; the anticipated size of the markets and continued demand for
the Company’s products and services; the impact of competitive services, products and pricing; and access to available financing
on a timely basis and on reasonable terms. We caution you that the foregoing list of important factors that may affect future results
is not exhaustive.
When
relying on forward-looking statements to make decisions with respect to the Company, investors and others should carefully consider the
foregoing factors and other uncertainties and potential events and read the Company’s filings with the SEC for a discussion of
these and other risks and uncertainties. The Company undertakes no obligation to update or revise any forward-looking statement, except
as may be required by law. The Company qualifies all forward-looking statements by these cautionary statements.
USE
OF PROCEEDS
We
will incur all costs associated with this registration statement and prospectus, which we anticipate to be approximately $25,500. We
will not receive any proceeds from the sale of our common stock covered hereby by any of the Selling Stockholders. We may receive proceeds
from the cash exercise of the Class B Warrants which, if exercised in full in cash, would result in gross proceeds of $898,029.
The shares of common stock to be sold in this offering have not yet been issued and will only be issued upon exercise of the Class B
Warrants.
MARKET
PRICE FOR COMMON EQUITY AND RELATED STOCKHOLDER MATTERS
Market
Information
Since
October 25, 2017, our common stock has been traded on the OTC Pink under the symbol “RNVA”. The following table sets forth
the high and low closing sales prices per share of our common stock as reported for the periods indicated, as adjusted to reflect all
applicable reverse stock splits. Such quotations represent inter-dealer prices without retail markup, markdown or commissions and may
not necessarily represent actual transactions. On May 10, 2023, the closing price for our common stock as reported on the OTC
Pink was $0.0001 per share.
Quarter
Ended | |
High | | |
Low | |
March
31, 2020 | |
$ | 20,000,000.00 | | |
$ | 10,000,000.00 | |
June
30, 2020 | |
$ | 30,000,000.00 | | |
$ | 5,000,000.00 | |
September
30, 2020 | |
$ | 30,000,000.00 | | |
$ | 1,700,000.00 | |
December
31, 2020 | |
$ | 2,500,000.00 | | |
$ | 130,000.00 | |
March
31, 2021 | |
$ | 380,000.00 | | |
$ | 40,800.00 | |
June
30, 2021 | |
$ | 60,000.00 | | |
$ | 4,000.00 | |
September
30, 2021 | |
$ | 8,000.00 | | |
$ | 2.00 | |
December
31, 2021 | |
$ | 9.00 | | |
$ | 0.50 | |
March
31, 2022 | |
$ | 1.00 | | |
$ | 0.010 | |
June
30, 2022 | |
$ | 0.0386 | | |
$ | 0.0001 | |
September
30, 2022 | |
$ | 0.0002 | | |
$ | 0.0001 | |
December
31, 2022 | |
$ | 0.0002 | | |
$ | 0.0001 | |
March 31, 2023 | |
$ | 0.0001 | | |
$ | 0.0001 | |
June 30, 2023 (through May 10, 2023) | |
$ | 0.0001 | | |
$ | 0.0001 | |
As
of May 1, 2023, there were two stockholders of record of our common stock, which excludes stockholders whose shares were held
in nominee or street name by brokers.
Voting
Agreement
Mr.
Diamantis, a former member of our Board of Directors, is the holder of our Series M Preferred Stock. On August 13, 2020, Mr. Diamantis
entered into a Voting Agreement and Irrevocable Proxy (the “Voting Agreement”) with the Company, Seamus Lagan and Alcimede
LLC (of which Mr. Lagan, the Company’s Chief Executive Officer, is the sole manager) pursuant to which Mr. Diamantis granted an
irrevocable proxy to Mr. Lagan to vote the Series M Preferred Stock held by Mr. Diamantis. Mr. Diamantis has retained all other rights
under the Series M Preferred Stock. Regardless of the number of shares of Series M Preferred Stock outstanding and so long as at least
one share of Series M Preferred Stock is outstanding, the outstanding shares of Series M Preferred Stock shall have the number of votes,
in the aggregate, equal to 51% of all votes entitled to be voted at any meeting of stockholders or action by written consent. This means
that the holders of Series M Preferred Stock have sufficient votes, by themselves, to approve or defeat any proposal voted on by the
Company’s stockholders, unless there is a supermajority required under applicable law or by agreement.
Dividend
Policy
Holders
of the Company’s common stock are entitled to dividends when, as, and if declared by the board of directors out of funds legally
available. The holders of the Rennova Series H Preferred Stock receive dividends at the same time any dividend is paid on shares
of common stock in an amount equal to the amount such holder would have received if such shares of preferred stock were converted into
common stock. Except for stock dividends, the holders of Rennova’s Series L Preferred Stock are not entitled to receive dividends
on their shares. For each of Rennova’s Series M Preferred Stock, Series N Preferred Stock, Series O Preferred Stock and Series
P Preferred Stock, dividends at the rate per annum of 10% of the stated value per share accrue on each outstanding share from and after
the date of the original issuance of such share. Such accruing dividends accrue from day to day, whether or not declared, and are cumulative
and non-compounding, provided, however, that such accruing dividends are payable only when, as and if declared by the Company’s
Board of Directors. No cash dividends may be paid on the common stock unless these accruing dividends are paid.
We
have never declared or paid any cash dividends on our common stock, nor do we anticipate any cash dividends on our common stock in the
foreseeable future. Certain of our financing agreements prohibit the payment of cash dividends.
The
Company intends to retain earnings, if any, to finance the development and expansion of its business. Future dividend policy will be
subject to the discretion of the board of directors and will be contingent upon future earnings, if any, the Company’s financial
condition, capital requirements, general business conditions, restrictions under the Company’s financing agreements and other factors.
Therefore, there can be no assurance that any dividends of any kind will ever be paid on the Company’s common stock.
BUSINESS
You
should read the following discussion and analysis of our financial condition and results of operations together with our financial statements
and related notes incorporated by reference in this prospectus. This discussion and analysis contains forward-looking statements that
involve risks, uncertainties and assumptions. The actual results may differ materially from those anticipated in these forward-looking
statements as a result of certain factors, including those set forth under “Risk Factors” and elsewhere in this prospectus.
See “Cautionary Note Regarding Forward-Looking Statements.”
Rennova
Health, Inc. (“Rennova” or the “Company”) is a provider of healthcare services. We own one operating
hospital in Oneida, Tennessee, a hospital located in Jamestown, Tennessee that we plan to reopen and operate, and a rural health clinic in Kentucky. The Company’s operations consist
of only one business segment, Hospital Operations.
Hospital
Operations
We
believe that the acquisition or development of rural hospitals and related healthcare services assets is a viable business strategy
and will create a stable revenue base from the provision of a needed service in rural America. These facilities deliver needed
healthcare services and employment to communities that would otherwise have to travel an hour or more to alternative locations.
Our
current operations began on August 8, 2017, following the receipt of the required licenses and regulatory approvals to open our
first hospital in Oneida, Tennessee. We had net revenues of approximately $13.0 million and approximately $3.2 million
during the years ended December 31, 2022 and 2021, respectively.
Scott
County Community Hospital (d/b/a Big South Fork Medical Center)
On
January 13, 2017, we acquired certain assets related to Scott County Community Hospital, based in Oneida, Tennessee (the “Oneida
Assets”). The Oneida Assets include a 52,000 square foot hospital building and 6,300 square foot professional building on approximately
4.3 acres. Scott County Community Hospital has 25 beds, a 24/7 emergency department and a laboratory that provides a range of diagnostic
services. Scott County Community Hospital closed in July 2016 in connection with the bankruptcy filing of its parent company, Pioneer
Health Services, Inc. We acquired the Oneida Assets out of bankruptcy for a purchase price of $1.0 million. The hospital, which has been
renamed Big South Fork Medical Center, became operational on August 8, 2017. The hospital became certified as a Critical Access Hospital in December 2021, retroactive to June 30, 2021.
Jamestown
Regional Medical Center
On
June 1, 2018, we acquired from Community Health Systems, Inc. certain assets related to an acute care hospital located in Jamestown,
Tennessee, referred to as Jamestown Regional Medical Center, for a purchase price of $0.7 million. The hospital is an 85-bed facility
of approximately 90,000 square feet on over eight acres of land, which offered a 24-hour emergency department with two trauma bays and
seven private exam rooms, inpatient and outpatient medical services and a progressive care unit which provided telemetry services. The
acquisition also included a separate physician practice known as Mountain View Physician Practice, Inc.
The
Company suspended operations at the hospital and physician practice in June 2019, as a result of the termination of the hospital’s
Medicare agreement and other factors. The Company is evaluating whether to reopen the facility as an acute care hospital or as another
type of healthcare facility. Jamestown is located 38 miles west of Big South fork Medical Center.
Jellico
Medical Center
On
March 5, 2019, we acquired certain assets related to a 54-bed acute care hospital that offered comprehensive services located in Jellico,
Tennessee known as Jellico Community Hospital and an outpatient clinic located in Williamsburg, Kentucky known as the CarePlus Center.
The hospital and the clinic and their associated assets were acquired from Jellico Community Hospital, Inc. and CarePlus Rural Health
Clinic, LLC, respectively. On
March 1, 2021, the Company closed Jellico Community Hospital, after the City of Jellico issued a 30-day termination notice for the lease
of the building.
The
CarePlus Clinic offers compassionate care in a modern, patient-friendly facility. The CarePlus Clinic is located 32 miles northwest of
our Big South Fork Medical Center.
Discontinued
Operations
Sale
of Health Technology Solutions, Inc. and Advanced Molecular Services Group, Inc.
On
June 25, 2021, the Company sold its subsidiaries, Health Technology Solutions, Inc. (“HTS”) and Advanced Molecular Services
Group, Inc. (“AMSG”), including their subsidiaries, to InnovaQor, Inc. (“InnovaQor”), formerly known as VisualMED
Clinical Solutions Corporation. HTS and AMSG held Rennova’s software and genetic testing interpretation divisions. In consideration
for the shares of HTS and AMSG and the elimination of intercompany debt among the Company and HTS and AMSG, InnovaQor issued the Company
14,950 shares of its Series B-1 Non-Voting Convertible Preferred Stock (the “InnovaQor Series B-1 Preferred Stock”). The
Company recorded a gain on the sale of HTS and AMSG of $11.3 million in the year ended December 31, 2021, of which $9.1 million
resulted from the value of the 14,950 shares of the InnovaQor Series B-1 Preferred Stock and $2.2 million resulted from the transfer
to InnovaQor of the net liabilities of HTS and AMSG. We have
reflected the financial results of HTS and AMSG prior to the sale, as well as the gain on sales, as discontinued operations in our consolidated
financial statements incorporated by reference herein.
EPIC
Reference Labs, Inc.
During
the third quarter of 2020, we made a decision to sell EPIC Reference Labs, Inc. (“EPIC”) and to discontinue several other
non-operating subsidiaries, and as a result, EPIC’s operations and the other non-operating subsidiaries’ liabilities have
been included in discontinued operations in the consolidated financial statements incorporated by reference in this prospectus. We were
unable to find a buyer for EPIC and, therefore, have ceased all efforts to sell EPIC and closed down its operations.
Outlook
Rural
healthcare facilities provide a much-needed service to their local communities. Furthermore, owning a number of facilities in the same
geographic location will create numerous efficiencies in management, purchasing and staffing and will enable the provision of additional,
specialized and more valuable services that are needed by rural communities but cannot be sustained by a standalone facilities. We remain
confident that this is a sustainable model we can continue to grow through acquisition and development.
In
the second quarter of 2022, we formed a subsidiary, Myrtle Recovery Centers, Inc., to pursue opportunities in the behavioral sector initially
in our core, rural markets. We intend to focus on leveraging our existing physical locations and corporate and regional infrastructure
to offer behavioral services including, but not limited to, substance abuse treatment. Services will be provided on either an inpatient,
residential basis or an outpatient basis. The Company is finalizing its plans for these initiatives, which are subject to many factors,
including licensure and the hiring of clinical and operational staff. The Company intends to initially offer substance abuse services
at its Big South Fork Medical Center campus. The Company expects the facility to be open and operating in the second quarter of 2023
although there is no assurance that the Company will proceed with its plans.
Impact
of the Pandemic
The
COVID-19 pandemic was declared a global pandemic by the World Health Organization on March 11, 2020. We continue to closely monitor
the COVID-19 pandemic and its impact on our operations and we have taken steps intended to minimize the risk to our employees and
patients. These steps have increased our costs and our net revenues have been significantly adversely affected. As noted in Notes 1,
7 and 8 to the consolidated financial statements incorporated by reference in this prospectus, we have received Paycheck Protection
Program loans (“PPP Notes”) as well as Department of Health and Human Services (“HHS”) Provider Relief Funds
and employee retention credits from the federal government. If the COVID-19 pandemic continues for a further extended period, we
expect to incur significant losses and additional financial assistance may be required. Going forward, we are unable to determine
the extent to which the COVID-19 pandemic will continue to affect our business. Our ability to make estimates of the effect of the
COVID-19 pandemic on net revenues, expenses or changes in accounting judgments that have had or are reasonably likely to have a
material effect on our financial statements is currently limited. The nature and effect of the COVID-19 pandemic on our balance
sheet and results of operations will depend on the severity and length of the pandemic in our service areas; government activities
to mitigate the pandemic’s effect; regulatory changes in response to the pandemic, especially those affecting rural hospitals;
existing and potential government assistance that may be provided; and the requirements of Provider Relief Fund receipts, including
our ability to retain such funds as have been received.
The
COVID-19 pandemic and the steps taken by governments to seek to reduce its spread have severely impacted the economy and the health care
industry in particular. Hospitals have especially been affected. Small rural hospitals, such as ours, may be overwhelmed by patients
if conditions worsen in their local areas. Staffing costs, and concerns due to the potential exposure to infections, may increase, as
may the costs of needed medical supplies necessary to keep the hospitals open. Doctors and patients may defer elective procedures and
other health care services. Travel bans, social distancing and quarantines may limit access to our facilities. Business closings and
layoffs in our local areas may result in the loss of insurance and adversely affect demand for our services, as well as the ability of
patients and other payers to pay for services as rendered.
These
developments have had, and may continue to have, a material adverse effect on us and the operations of our hospitals.
Corporate
Information
Effective
November 2, 2015, the Company, a Delaware corporation, changed its name from “CollabRx, Inc.” to “Rennova Health, Inc.”
The Company was previously named Tegal Corporation until 2012 when it acquired a private company named CollabRx, Inc. and changed its
name to “CollabRx, Inc.” Tegal Corporation was formed in December 1989 to acquire the operations of the former Tegal Corporation,
a division of Motorola, Inc. Tegal’s predecessor company was founded in 1972 and was acquired by Motorola, Inc. in 1978. Tegal
completed its initial public offering in October 1995.
The
Company’s fiscal year-end is December 31.
Our
principal executive offices are located at 400 South Australian Avenue, Suite 800, West Palm Beach, Florida 33401 and our telephone number
is (561) 855-1626. Our website address is www.rennovahealth.com. The information contained on, or that can be accessed through, our website
is not part of this prospectus.
Competition
The
healthcare industry is highly competitive among hospitals and other healthcare providers for patients, affiliations with physicians and
acquisitions. The most significant competition our hospitals, and any other hospitals we may acquire, face comes from hospitals that
provide more complex services, and other healthcare providers, including outpatient surgery, orthopedic, oncology and diagnostic centers
that also compete for patients. Our hospitals, our competitors, and other healthcare industry participants are increasingly implementing
physician alignment strategies, such as acquiring physician practice groups, employing physicians and participating in accountable care
organizations (“ACOs”) or other clinical integration models, which may impact our competitive position. In addition, increasing
consolidation within the payor industry, vertical integration efforts involving payors and healthcare providers, and cost-reduction strategies
by large employer groups and their affiliates may impact our ability to contract with payors on favorable terms and otherwise affect
our competitive position.
Governmental
Regulation
Overview
The
healthcare industry is governed by an extremely complex framework of federal, state and local laws, rules and regulations, and there
continues to be federal and state proposals that would, and actions that do, impose limitations on government and private payments to
providers. In addition, there regularly are proposals to increase co-payments and deductibles from program and private patients. Facilities
also are affected by controls imposed by government and private payors designed to reduce admissions and lengths of stay. Such controls
include what is commonly referred to as “utilization review”. Utilization review entails the review of a patient’s
admission and course of treatment by a third party. Historically, utilization review has resulted in a decrease in certain treatments
and procedures being performed. Utilization review is required in connection with the provision of care which is to be funded by Medicare
and Medicaid and is also required under many managed care arrangements.
Many
states have enacted, or are considering enacting, additional measures that are designed to reduce their Medicaid expenditures and to
make changes to private healthcare insurance. Various states have applied, or are considering applying, for a waiver from current Medicaid
regulations in order to allow them to serve some of their Medicaid participants through managed care providers. These proposals also
may attempt to include coverage for some people who presently are uninsured, and generally could have the effect of reducing payments
to hospitals, physicians and other providers for the same level of service provided under Medicaid.
Healthcare
Facility Regulation
Certificate
of Need Requirements
A
number of states require approval for the purchase, construction or expansion of various healthcare facilities, including findings of
need for additional or expanded healthcare services. Certificates of Need (“CONs”), which are issued by governmental agencies
with jurisdiction over applicable healthcare facilities, are at times required for capital expenditures exceeding a prescribed amount,
changes in bed capacity or the addition of services and certain other matters. Tennessee, the state in which we currently own our hospitals,
has a CON law that applies to such facilities. States periodically review, modify and revise their CON laws and related regulations.
Any violation of state CON laws can result in the imposition of civil sanctions or the revocation of licenses for such facilities. We
are unable to predict whether our hospitals will be able to obtain any CONs that may be necessary to accomplish their business objectives
in any jurisdiction where such certificates of need are required. In addition, future healthcare facility acquisitions also may occur
in states that require CONs.
Future
healthcare facility acquisitions also may occur in states that do not require CONs or which have less stringent CON requirements than
the state in which Rennova currently owns hospitals. Any healthcare facility operated by the Company in such states may face increased
competition from new or expanding facilities operated by competitors, including physicians.
Utilization
Review Compliance and Hospital Governance
Healthcare
facilities are subject to, and are required to comply with, various forms of utilization review. In addition, under the Medicare prospective
payment system, each state must have a peer review organization to carry out a federally mandated system of review of Medicare patient
admissions, treatments and discharges in hospitals. Medical and surgical services and physician practices are supervised by committees
of staff doctors at each healthcare facility, are overseen by each healthcare facility’s local governing board, the primary voting
members of which are physicians and community members, and are reviewed by quality assurance personnel. The local governing boards also
help maintain standards for quality care, develop long-range plans, establish, review and enforce practices and procedures and approve
the credentials and disciplining of medical staff members.
Emergency
Medical Treatment and Active Labor Act
The
Emergency Medical Treatment and Active Labor Act (“EMTALA”) is a federal law that requires any hospital that participates
in the Medicare program to conduct an appropriate medical screening examination of every person who presents to the hospital’s
emergency department for treatment and, if the patient is suffering from an emergency medical condition or is in active labor, to either
stabilize that condition or make an appropriate transfer of the patient to a facility that can handle the condition. The obligation to
screen and stabilize emergency medical conditions exists regardless of a patient’s ability to pay for treatment. There are severe
penalties under EMTALA if a hospital fails to screen or appropriately stabilize or transfer a patient or if the hospital delays appropriate
treatment in order to first inquire about the patient’s ability to pay. Penalties for violations of EMTALA include civil monetary
penalties and exclusion from participation in the Medicare program, the Medicaid program or both. In addition, an injured patient, the
patient’s family or a medical facility that suffers a financial loss as a direct result of another hospital’s violation of
the law can bring a civil suit against that other hospital. Although we believe that we comply with EMTALA, we cannot predict whether
the Centers for Medicare & Medicaid Services (“CMS”) will implement new requirements in the future and whether we will
be able to comply with any new requirements.
Drugs
and Controlled Substances
Various
licenses and permits are required by our hospitals to dispense narcotics. They are required to register our dispensing operations for
permits and/or licenses with, and comply with certain operating and security standards of, the United States Drug Enforcement Agency
(“DEA”), the Food and Drug Administration (“FDA”), state health departments and other state agencies.
Fraud
and Abuse, Anti-Kickback and Self-Referral Regulations
Participation
in the Medicare and/or Medicaid programs is heavily regulated by federal statutes and regulations. If we fail to comply substantially
with the numerous federal laws governing our businesses, our participation in the Medicare and/or Medicaid programs may be terminated
and/or civil or criminal penalties may be imposed. For example, a hospital may lose its ability to participate in the Medicare and/or
Medicaid programs if it:
|
● |
makes
claims to Medicare and/or Medicaid for services not provided or misrepresents actual services provided in order to obtain higher
payments; |
|
|
|
|
● |
pays
money to induce the referral of patients or the purchase of items or services where such items or services are reimbursable under
a federal or state health program; |
|
|
|
|
● |
fails
to report or repay improper or excess payments; or |
|
|
|
|
● |
fails
to provide appropriate emergency medical screening services to any individual who comes to a hospital’s campus or otherwise
fails to properly treat and transfer emergency patients. |
Hospitals
continue to be one of the primary focus areas of the federal Office of the Inspector General (“OIG”) and other governmental
fraud and abuse programs and the OIG has issued and periodically updated compliance program guidance for hospitals. Each federal fiscal
year, the OIG also publishes a General Work Plan that provides a brief description of the activities that the OIG plans to initiate or
continue with respect to the programs and operations of HHS and details the areas that the OIG believes are prone to fraud and abuse.
Sections
of the Anti-Fraud and Abuse Amendments to the Social Security Act, commonly known as the “anti-kickback” statute, prohibit
certain business practices and relationships that might influence the provision and cost of healthcare services reimbursable under Medicare,
Medicaid, TriCare or other healthcare programs, including the payment or receipt of remuneration for the referral of patients whose care
will be funded by Medicare or other government programs. Sanctions for violating the anti-kickback statute include criminal penalties
and civil sanctions, including fines and possible exclusion from future participation in government programs, such as Medicare and Medicaid.
HHS has issued regulations that create safe harbors under the anti-kickback statute. A given business arrangement that does not fall
within an enumerated safe harbor is not per se illegal; however, business arrangements that fail to satisfy the applicable safe harbor
criteria are subject to increased scrutiny by enforcement authorities.
The
Health Insurance Portability and Accountability Act of 1996 (“HIPAA”) broadened the scope of the fraud and abuse laws by
adding several criminal statutes that are not related to receipt of payments from a federal healthcare program. HIPAA created civil penalties
for proscribed conduct, including upcoding and billing for medically unnecessary goods or services. These laws cover all health insurance
programs, private as well as governmental. In addition, HIPAA broadened the scope of certain fraud and abuse laws, such as the anti-kickback
statute, to include not just Medicare and Medicaid services, but all healthcare services reimbursed under a federal or state healthcare
program. Finally, HIPAA established enforcement mechanisms to combat fraud and abuse. These mechanisms include a bounty system where
a portion of the payment recovered is returned to the government agencies, as well as a whistleblower program, where a portion of the
payment received is paid to the whistleblower. HIPAA also expanded the categories of persons that may be excluded from participation
in federal and state healthcare programs.
There
is increasing scrutiny by law enforcement authorities, the OIG, the courts and the U.S. Congress of arrangements between healthcare providers
and potential referral sources to ensure that the arrangements are not designed as mechanisms to exchange remuneration for patient-care
referrals and opportunities. Investigators also have demonstrated a willingness to look behind the formalities of a business transaction
and to reinterpret the underlying purpose of payments between healthcare providers and potential referral sources. Enforcement actions
have increased, as is evidenced by highly publicized enforcement investigations of certain hospital activities.
In
addition, provisions of the Social Security Act, known as the Stark Act, also prohibit physicians from referring Medicare and Medicaid
patients to providers of a broad range of designated health services with which the physicians or their immediate family members have
ownership or certain other financial arrangements. Certain exceptions are available for employment agreements, leases, physician recruitment
and certain other physician arrangements. A person making a referral, or seeking payment for services referred, in violation of the Stark
Act is subject to civil monetary penalties; restitution of any amounts received for illegally billed claims; and/or exclusion from future
participation in the Medicare program, which can subject the person or entity to exclusion from future participation in state healthcare
programs.
Further,
if any physician or entity enters into an arrangement or scheme that the physician or entity knows or should have known has the principal
purpose of assuring referrals by the physician to a particular entity, and the physician directly makes referrals to such entity, then
such physician or entity could be subject to a civil monetary penalty. Compliance with and the enforcement of penalties for violations
of these laws and regulations is changing and increasing. For example, CMS has issued a “self-referral disclosure protocol”
for hospitals and other providers that wish to self-disclose potential violations of the Stark Act and attempt to resolve those potential
violations and any related overpayment liabilities at levels below the maximum penalties and amounts set forth in the statute. In light
of the provisions of the Affordable Care Act that created potential liabilities under the federal False Claims Act (discussed below)
for failing to report and repay known overpayments and return an overpayment within 60 days of the identification of the overpayment
or the date by which a corresponding cost report is due, whichever is later, hospitals and other healthcare providers are encouraged
to disclose potential violations of the Stark Act to CMS. It is likely that self-disclosure of Stark Act violations will increase in
the future. Finally, many states have adopted or are considering similar legislative proposals, some of which extend beyond the Medicaid
program, to prohibit the payment or receipt of remuneration for the referral of patients and physician self-referrals regardless of the
source of the payment for the care.
The
Federal False Claims Act and Similar State Laws
The
federal False Claims Act prohibits providers from, among other things, knowingly submitting false or fraudulent claims for payment to
the federal government. The False Claims Act defines the term “knowingly” broadly, and while simple negligence generally
will not give rise to liability, submitting a claim with reckless disregard to its truth or falsity can constitute the “knowing”
submission of a false or fraudulent claim for the purposes of the False Claims Act. The “qui tam” or “whistleblower”
provisions of the False Claims Act allow private individuals to bring actions under the False Claims Act on behalf of the government.
These private parties are entitled to share in any amounts recovered by the government, and, as a result, the number of “whistleblower”
lawsuits that have been filed against providers has increased significantly in recent years. When a private party brings a qui
tam action under the False Claims Act, the defendant will generally not be aware of the lawsuit until the government makes a
determination whether it will intervene and take a lead in the litigation. If a provider is found to be liable under the False Claims
Act, the provider may be required to pay up to three times the actual damages sustained by the government plus mandatory civil monetary
penalties for each separate false claim. The government has used the False Claims Act to prosecute Medicare and other government healthcare
program fraud such as coding errors, billing for services not provided, submitting false cost reports, and providing care that is not
medically necessary or that is substandard in quality. A qui tam lawsuit has been filed against the Company alleging violations
of the False Claims Act. See “Legal Proceedings”.
HIPAA
Transaction, Privacy and Security Requirements
HIPAA
and federal regulations issued pursuant to HIPAA contain, among other measures, provisions that have required the Company to implement
modified or new computer systems, employee training programs and business procedures. The federal regulations are intended to encourage
electronic commerce in the healthcare industry, provide for the confidentiality and privacy of patient healthcare information and ensure
the security of healthcare information.
A
violation of the HIPAA regulations could result in civil money penalties per standard violated. HIPAA also provides for criminal penalties
and one year in prison for knowingly and improperly obtaining or disclosing protected health information, up to five years in prison
for obtaining protected health information under false pretenses and up to ten years in prison for obtaining or disclosing protected
health information with the intent to sell, transfer or use such information for commercial advantage, personal gain or malicious harm.
Since there is limited history of enforcement efforts by the federal government at this time, it is difficult to ascertain the likelihood
of enforcement efforts in connection with the HIPAA regulations or the potential for fines and penalties, which may result from any violation
of the regulations.
HIPAA
Privacy Regulations
HIPAA
privacy regulations protect the privacy of individually identifiable health information. The regulations provide increased patient control
over medical records, mandate substantial financial penalties for violation of a patient’s right to privacy and, with a few exceptions,
require that an individual’s individually identifiable health information only be used for healthcare-related purposes. These privacy
standards apply to all health plans, all healthcare clearinghouses and all healthcare providers, such as our hospitals, that transmit
health information in an electronic form in connection with standard transactions and apply to individually identifiable information
held or disclosed by a covered entity in any form. These standards impose extensive administrative requirements on our hospitals and
require compliance with rules governing the use and disclosure of such health information, and they require our facilities to impose
these rules, by contract, on any business associate to whom we disclose such information in order to perform functions on our behalf.
In addition, our hospitals are subject to any state laws that are more restrictive than the privacy regulations issued under HIPAA. These
laws vary by state and could impose stricter standards and additional penalties.
The
HIPAA privacy regulations also require healthcare providers to implement and enforce privacy policies to ensure compliance with the regulations
and standards. We believe all of our facilities are in compliance with current HIPAA privacy regulations.
HIPAA
Electronic Data Standards
The
Administrative Simplification Provisions of HIPAA require the use of uniform electronic data transmission standards for all healthcare
related electronic data interchange. These provisions are intended to streamline and encourage electronic commerce in the healthcare
industry. Among other things, these provisions require us to use standard data formats and code sets established by HHS when electronically
transmitting information in connection with certain transactions, including health claims and equivalent encounter information, healthcare
payment and remittance advice and health claim status.
The
HHS regulations establish electronic data transmission standards that all healthcare providers and payors must use when submitting and
receiving certain electronic healthcare transactions. The uniform data transmission standards are designed to enable healthcare providers
to exchange billing and payment information directly with the many payors thereby eliminating data clearinghouses and simplifying the
interface programs necessary to perform this function. We believe that our management information systems comply with HIPAA’s electronic
data regulations and standards.
HIPAA
Security Standards
The
Administrative Simplification Provisions of HIPAA require the use of a series of security standards for the protection of electronic
health information. The HIPAA security standards rule specifies a series of administrative, technical and physical security procedures
for covered entities to use to assure the confidentiality of electronic protected health information. The standards are delineated into
either required or addressable implementation specifications. We believe we are in compliance with all the aspects of the HIPAA security
regulations.
HIPAA
National Provider Identifier
HIPAA
also required HHS to issue regulations establishing standard unique health identifiers for individuals, employers, health plans and healthcare
providers to be used in connection with standard electronic transactions. All healthcare providers, including our hospitals, were required
to obtain a new National Provider Identifier (“NPI”) to be used in standard transactions instead of other numerical identifiers
by May 23, 2007. Our hospitals implemented use of a standard unique healthcare identifier by utilizing their employer identification
number. HHS has not yet issued proposed rules that establish the standard for unique health identifiers for health plans or individuals.
Once these regulations are issued in final form, we expect to have approximately one to two years to become fully compliant, but cannot
predict the impact of such changes at this time. We cannot predict whether our facilities may experience payment delays during the transition
to the new identifiers. HHS is currently working on the standards for identifiers for health plans; however, there are currently no proposed
timelines for issuance of proposed or final rules. The issuance of proposed rules for individuals is on hold indefinitely.
Medical
Waste Regulations
Our
operations, especially our hospitals, generate medical waste that must be disposed of in compliance with federal, state and local environmental
laws, rules and regulations. Our operations are also generally subject to various other environmental laws, rules and regulations. Based
on our current level of operations, we do not anticipate that such compliance costs will have a material adverse effect on our cash flows,
financial position or results of operations.
Compliance
Program
The
Company continuously evaluates and monitors its compliance with all Medicare, Medicaid and other rules and regulations. The objective
of the Company’s compliance program is to develop, implement and update compliance safeguards as necessary. Emphasis is placed
on developing and implementing compliance policies and guidelines, personnel training programs and various monitoring and audit procedures
to attempt to achieve implementation of all applicable rules and regulations.
The
Company seeks to conduct its business in compliance with all statutes, regulations, and other requirements applicable to its operations.
The health care industry is, however, subject to extensive regulation, and many of these statutes and regulations have not been interpreted
by the courts. There can be no assurance that applicable statutes and regulations will not be interpreted or applied by a prosecutorial,
regulatory or judicial authority in a manner that would adversely affect the Company. Potential sanctions for violation of these statutes
and regulations include significant civil and criminal penalties, fines, exclusions from participation in government health care programs
and the loss of various licenses, certificates and authorizations, necessary to operate as well as potential liabilities from third-party
claims, all of which could have a material adverse effect on the Company’s business.
Professional
Liability
As
part of our business, our facilities are subject to claims of liability for events occurring in the ordinary course of operations. Professional
malpractice liability insurance and general liability insurance policies are maintained in amounts which are commercially available
and believed to be sufficient for operations as currently conducted, although some claims may exceed the scope or amount of the coverage
in effect.
Environmental
Regulation
We
believe we are in substantial compliance with applicable federal, state and local environmental regulations. To date, compliance with
federal, state and local laws regulating the discharge of material into the environment or otherwise relating to the protection of the
environment have not had a material effect upon our results of operations, financial condition or competitive position. Similarly, we
have not had to make material capital expenditures to comply with such regulations.
Payment
for Services
The
Company’s hospital operations depend significantly on continued participation in the Medicare and Medicaid programs and in other
government healthcare programs. In recent years, both governmental and private sector payers have made efforts to contain or reduce health
care costs, including reducing reimbursement for services.
Under
the Consolidated Appropriations Act of 2021, effective as of January 1, 2022, Congress adopted provisions to help protect patients against
surprise bills and provide more price transparency. Patients have new billing protections when receiving emergency care and non-emergency
care from out-of-network providers at in-network facilities. Excessive out-of-pocket costs are restricted and emergency services must
continue to be covered without any prior authorization and regardless of whether or not a provider or facility is in-network.
Further
healthcare reform could occur, including changes to the Affordable Care Act and Medicare reform, as well as administrative requirements
that may affect coverage, reimbursement and utilization of our hospitals in ways that are currently unpredictable.
Employees
On
March 30, 2023, we had 128 employees, of which 85 were full time. None of the Company’s employees are
represented by a union.
Legal
Proceedings
From
time to time, the Company may be involved in a variety of claims, lawsuits, investigations and proceedings related to contractual disputes,
employment matters, regulatory and compliance matters, intellectual property rights and other litigation arising in the ordinary course
of business. The Company operates in a highly regulated industry which may inherently lend itself to legal matters. Management is aware
that litigation has associated costs and that results of adverse litigation verdicts could have a material effect on the Company’s
financial position or results of operations. The Company’s policy is to expense legal fees and expenses incurred in connection
with the legal proceedings in the period in which the expense is incurred. Management, in consultation with legal counsel, has addressed
known assertions and predicted unasserted claims below.
Biohealth
Medical Laboratory, Inc. and PB Laboratories, LLC (the “Companies”) filed suit against CIGNA Health in 2015 alleging that
CIGNA failed to pay claims for laboratory services the Companies provided to patients pursuant to CIGNA - issued and CIGNA - administered
plans. In 2016, the U.S. District Court dismissed part of the Companies’ claims for lack of standing. The Companies appealed that
decision to the Eleventh Circuit Court of Appeals, which in late 2017 reversed the District Court’s decision and found that the
Companies have standing to raise claims arising out of traditional insurance plans as well as self-funded plans. In July 2019, the Companies
and EPIC filed suit against CIGNA Health for failure to pay claims for laboratory services provided. Cigna Health, in turn, sued for
alleged improper billing practices. The suit remains ongoing but because the Company did not have the financial resources to see the
legal action to conclusion it assigned the benefit, if any, from the suit to Mr. Diamantis for his financial support to the Company and
assumption of all costs to carry the case to conclusion.
On
September 27, 2016, a tax warrant was issued against the Company by the Florida Department of Revenue (the “DOR”) for unpaid
2014 state income taxes in the approximate amount of $0.9 million, including penalties and interest. The Company entered into a Stipulation
Agreement with the DOR allowing the Company to make monthly installments until July 2019. The Company has made payments to reduce the
amount owed. The balance accrued of approximately $0.4 million remained outstanding to the DOR at December 31, 2022.
On
December 7, 2016, the holders of the Tegal Notes (see Note 8 to the consolidated financial statements incorporated by
reference in this prospectus) filed suit against the Company seeking payment for the amounts due under the notes in the aggregate principal
balance of $341,612, and accrued interest of $43,000. A request for entry of default judgment was filed on January 24, 2017. On April
23, 2018, the holders of the Tegal Notes received a judgment against the Company. As of December 31, 2022, the Company has repaid
$50,055 of the principal amount of these notes.
The
Company, as well as many of its subsidiaries, were defendants in a case filed in Broward County Circuit Court by TCA Global Credit Master
Fund, L.P. The plaintiff alleged a breach by Medytox Solutions, Inc. of its obligations under a debenture and claimed damages of approximately
$2,030,000 plus interest, costs and fees. The Company and the other subsidiaries were sued as alleged guarantors of the debenture. The
complaint was filed on August 1, 2018. In May 2020, the SEC appointed a Receiver to close down the TCA Global Credit Master Fund, L.P.
The Company and the Receiver entered into a settlement agreement dated effective as of September 30, 2021, under which the Company agreed
to pay $500,000 as full and final settlement of principal and interest, of which $200,000 was paid on November 4, 2021 and the remaining
$300,000 was due in six consecutive monthly installments of $50,000. Accordingly, the settlement amount was fully paid as of December
31, 2022 (see Note 8 to the consolidated financial statements incorporated by reference in this prospectus).
As a result of the settlement, the Company recorded a gain from legal settlement of $2.2 million in the year ended December 31, 2021.
On
September 13, 2018, Laboratory Corporation of America sued EPIC, a subsidiary of the Company, in Palm Beach County Circuit Court for
amounts claimed to be owed. The court awarded a judgment against EPIC in May 2019 for approximately $155,000. The Company has recorded
the amount owed as a liability as of December 31, 2022.
In
February 2020, Anthony O’Killough sued the Company and Mr. Diamantis, as guarantor, in New York State Supreme Court for the
County of New York, for approximately $2.0 million relating to the promissory note issued by the Company in September 2019. In May
2020, the Company, Mr. Diamantis, as guarantor, and Mr. O’Killough entered into a Stipulation providing for a payment of a
total of $2.2 million (which included accrued “penalty” interest as of that date) in installments through November 1,
2020. The Company made payments totaling $450,000 in 2020. On January 18, 2022, Mr. Diamantis paid $750,000 and the remaining
balance was due 120 days thereafter. Mr. O’Killough agreed to forebear from any further enforcement action until then. On
various dates during the remainder of 2022, Mr. Diamantis made additional payments to Mr. O’Killough totalling $300,000 and
the Company gave Mr. Diamantis $350,000 for further payment to Mr. O’Killough. As a result of these payments, the past due
balance owed to Mr. O’Killough was $1.1 million on December 31, 2022, The Company is obligated to repay Mr. Diamantis for
any payments, plus interest, that he made to Mr. O,Killough. On January 27, 2023, the parties entered into a final
settlement wherein the Company and Mr. Diamantis agreed to settle the obligation in full for $580,000. The promissory note,
forbearance agreement and final settlement are also discussed in Notes 8, 14 and 18 to the consolidated financial statements
incorporated by reference in this prospectus.
In
June 2019, CHSPSC, the former owners of Jamestown Regional Medical Center, obtained a judgment against the Company in the amount of $592,650.
The Company has recorded this judgment as a liability as of December 31, 2022. However, management believes that a number of insurance
payments were made to CHSPSC for services provided after the change of ownership and believes that these payments will offset portions of the judgment.
In
August 2019, Morrison Management Specialists, Inc. obtained a judgment against Jamestown Regional Medical Center and the Company in Fentress
County, Tennessee in the amount of $194,455 in connection with housekeeping and dietary services. The Company has recorded this liability
as of December 31, 2022.
In
November 2019, Newstat, PLLC obtained a judgment against Big South Fork Medical Center in Knox County, Tennessee in the amount of $190,600
in connection with the provision of medical services. On February 15, 2023, the Company and Newstat agreed to settle the amount owed
for $210,000 in four equal monthly payments of $52,500 beginning February 2023. The Company has made the payments under the settlement
agreement to date. The Company has recorded the $210,000 as a liability as of December 31, 2022.
On
June 30, 2021, the Company entered into a settlement agreement with the Tennessee Bureau of Workers’ Compensation. Per the terms
of the settlement agreement, the Company is obligated to pay a total of $109,739, payable in a lump sum payment of $32,922 on or before
August 15, 2021 and in 24 consecutive monthly payments of $3,201 each on or before the 15th day of each month beginning September
15, 2021. The Company has made the required payments due as of December 31, 2022 and has recorded the remaining amounts owed as
a liability as of December 31, 2022.
In
July 2021, WG Fund, Queen Funding and Diesel Funding filed legal actions in New York State Supreme Court for Kings County to recover
amounts claimed to be outstanding on accounts receivable sales agreements entered into in 2020. On September 14, 2021, the Company entered
into separate stipulation of settlement agreements with the three funding parties under which the Company agreed to repay an aggregate
of $0.9 million in equal monthly payments totaling $52,941 through January 1, 2023. As of December 31, 2022, the settlement amounts
were paid in full.
A sealed
qui tam lawsuit in the U.S. District Court for the Southern District of Florida against the Company was filed in July 2021. This
lawsuit was unsealed in November 2022 and Clifford Barron disclosed as the Plaintiff-Relator asserting violations of the False Claims
Act. Clifford Barron was an employee of CollabRx, Inc. (a San Francisco based, wholly owned subsidiary of the Company) until early 2018.
Following his resignation on January 17, 2018, Clifford Barron sought and received a judgment against the Company for approximately $253,000
he claimed was owed to him by the CollabRx subsidiary for severance and payment of COBRA. On receiving the judgment, he collected all
monies owed to him under this judgment, including from the Company’s rural healthcare operations in Tennessee with which he was
not involved. Payments included approximately $164,000 secured from hospital operating and other bank accounts by garnishments initiated
by Jonathan Swann Taylor of Taylor & Knight, GP, Knoxville Tennessee, on behalf of Clifford Barron in May 2022. Clifford Barron has
not been an employee of any subsidiary of the Company since January 2018, is not involved with the Company and has no knowledge of the
Company’s operations, financial status, or controls. On November 21, 2022, the Company was advised that the U.S. Department of
Justice has intervened in the action filed by the Plaintiff-Relator, Clifford Barron and has requested repayment of HHS Provider Relief
Funds that certain subsidiaries of the Company obtained and other relief. The Company has retained the services of a specialist third-party
accounting firm to complete a forensic review of the expenditure of all monies expended since the receipt of HHS Provider Relief Funds.
It has been discovered that certain filing requirements of the Company’s operating subsidiaries were incomplete or contained errors
that did not accurately reflect the expenditure of HHS Provider Relief Funds received. The Company disputes the allegations made and
believes that the forensic review of funds expended will address the lawsuit and demonstrate adherence with the applicable rules for
use of HHS Provider Relief Funds. Accordingly, no amount has been accrued for this potential liability at December 31, 2022. There is
no assurance that the Company will be able to retain all HHS Provider Relief Funds it has received nor avoid payment of other relief
sought by the Department of Justice. Any requirement to repay a significant amount of HHS Provider Relief Funds could have a material
adverse effect on the Company.
MANAGEMENT’S
DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION
AND RESULTS OF OPERATIONS
The
following discussion and analysis provide information which management believes is relevant to an assessment and understanding of our
consolidated results of operations and financial condition. This discussion contains forward-looking statements that involve risks and
uncertainties. Our actual results may differ materially from those anticipated in these forward-looking statements as a result of numerous
factors including, but not limited to, those described above under “Cautionary Statement Concerning Forward-Looking Statements”
and “Risk Factors”. The discussion should be read in conjunction with the financial statements and notes thereto incorporated
by reference in this prospectus.
Unless
stated otherwise, the words “we,” “us,” “our,” “the Company,” “Rennova Health”
or “Rennova Health, Inc.,” means Rennova Health, Inc.
RESULTS
OF OPERATIONS
Critical
Accounting Policies and Estimates
Our
discussion and analysis of financial condition and results of operations are based on our consolidated financial statements, which have
been prepared in accordance with accounting principles generally accepted in the United States of America (“U.S. GAAP”).
The preparation of these financial statements requires us to make a number of estimates and assumptions that affect the reported amounts
of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements. Such estimates
and assumptions affect the reported amounts of revenues and expenses during the reporting period. We base our estimates on historical
experiences and on various other assumptions that we believe to be reasonable under the circumstances. Actual results may differ materially
from these estimates under different assumptions and conditions. We continue to monitor significant estimates made during the preparation
of our financial statements. On an ongoing basis, we evaluate estimates and assumptions based upon historical experience and various
other factors and circumstances.
We
have identified the policies and significant estimation processes discussed below as critical to our business and to the understanding
of our results of operations. For a detailed application of these and other accounting policies, see Note 2 to the consolidated
financial statements as of and for the year ended December 31, 2022 incorporated by reference in this prospectus.
Revenue
Recognition
We
recognize revenue in accordance with Accounting Standard Update (“ASU”) 2014-09, “Revenue from Contracts with Customers
(Topic 606),” including subsequently issued updates. Under the accounting guidance, we no longer present the provision for
doubtful accounts as a separate line item and our revenues are presented net of estimated contractual allowances. We also do not present
“allowances for doubtful accounts” on our balance sheets.
Our
revenues relate to contracts with patients in which our performance obligations are to provide health care services to the patients.
Revenues are recorded during the period that our obligations to provide health care services are satisfied. Our performance
obligations for inpatient services are generally satisfied over periods averaging approximately three days, and revenues are
recognized based on charges incurred. Our performance obligations for outpatient services, including emergency room-related
services, are generally satisfied over a period of less than one day. The contractual relationships with patients, in most cases,
also involve a third-party payer (Medicare, Medicaid, managed care health plans and commercial insurance companies, including plans
offered through the health insurance exchanges) and the transaction prices for the services provided are dependent upon the terms
provided by (Medicare and Medicaid) or negotiated with (managed care health plans and commercial insurance companies) the
third-party payers. The payment arrangements with third-party payers for the services we provide to the related patients typically
specify payments at amounts less than our standard charges. Medicare, because of the Big South Fork Medical Center’s
designation as a Critical Access Hospital, generally pays for inpatient and outpatient services at rates related to the
hospital’s costs. Services provided to patients having Medicaid coverage are generally paid at prospectively determined rates
per discharge, per identified service or per covered member. Agreements with commercial insurance carriers, managed care and
preferred provider organizations generally provide for payments based upon predetermined rates per diagnosis, per diem rates or
discounted fee-for-service rates. Management continually reviews the contractual estimation process to consider and incorporate
updates to laws and regulations and the frequent changes in managed care contractual terms resulting from contract renegotiations
and renewals. Our net revenues are based upon the estimated amounts we expect to be entitled to receive from patients and
third-party payers. Estimates of contractual allowances under managed care and commercial insurance plans are based upon the payment
terms specified in the related contractual agreements. Revenues related to uninsured patients and uninsured copayment and deductible
amounts for patients who have health care coverage may have discounts applied (uninsured discounts and contractual discounts). We
also record estimated implicit price concessions (based primarily on historical collection experience) related to uninsured accounts
to record self-pay revenues at the estimated amounts we expect to collect.
Laws
and regulations governing the Medicare and Medicaid programs are complex and subject to interpretation. Estimated reimbursement amounts
are adjusted in subsequent periods as cost reports are prepared and filed and as final settlements are determined (in relation to certain
government programs, primarily Medicare, this is generally referred to as the “cost report” filing and settlement process).
During the fourth quarter of 2022, the Company’s Big South Fork Medical Center received a communication that its final Medicare
cost report for the six months ending December 31, 2021 was accepted and that it reflected a retroactive adjustment of $1.6 million as
a result of an overpayment. Accordingly, we have reflected the $1.6 million cost report adjustment as a liability at December 31, 2022.
Furthermore, the Company recognized an additional $0.5 million as a liability (net of recoupments) at December 31, 2022 based on further
correspondence with its fiscal intermediary and likely overpayments by Medicare for fiscal 2022.
The
collection of outstanding receivables for Medicare, Medicaid, managed care payers, other third-party payers and patients is our primary
source of operating cash and is critical to our operating performance. The primary collection risks relate to uninsured patient accounts,
including patient accounts for which the primary insurance carrier has paid the amounts covered by the applicable agreement, but patient
responsibility amounts (deductibles and copayments) remain outstanding. Implicit price concessions relate primarily to amounts due directly
from patients. Estimated implicit price concessions are recorded for all uninsured accounts, regardless of the aging of those accounts.
Accounts are written off when all reasonable internal and external collection efforts have been performed. The estimates for implicit
price concessions are based upon management’s assessment of historical write offs and expected net collections, business and economic
conditions, trends in federal, state and private employer health care coverage and other collection indicators. Management relies on
the results of detailed reviews of historical write-offs and collections at facilities that represent a majority of our revenues and
accounts receivable (the “hindsight analysis”) as a primary source of information in estimating the collectability of our
accounts receivable.
Contractual
Allowances and Doubtful Accounts Policy
Accounts
receivable are reported at realizable value, net of estimated contractual allowances and estimated implicit price concessions (also referred
to as doubtful accounts), which are estimated and recorded in the period the related revenue is recorded. The Company has a standardized
approach to estimating and reviewing the collectability of its receivables based on a number of factors, including the period they have
been outstanding. Historical collection and payer reimbursement experience is an integral part of the estimation process related to contractual
allowances and doubtful accounts. In addition, the Company regularly assesses the state of its billing operations in order to identify
issues which may impact the receivables or reserve estimates. Receivables deemed to be uncollectible are charged against the allowance
for doubtful accounts at the time such receivables are written-off. Recoveries of receivables previously written-off are recorded as
credits to the allowance for doubtful accounts. Revisions to the allowances for doubtful accounts are recorded as an adjustment to revenues.
Impairment
or Disposal of Long-Lived Assets
We
account for the impairment or disposal of long-lived assets according to the Financial Accounting Standards Board (the “FASB”)
Accounting Standards Codification (“ASC”) Topic 360, Property, Plant and Equipment (“ASC 360”). ASC 360
clarifies the accounting for the impairment of long-lived assets and for long-lived assets to be disposed of, including the disposal
of business segments and major lines of business. Long-lived assets are reviewed when facts and circumstances indicate that the carrying
value of the asset may not be recoverable. When necessary, impaired assets are written down to estimated fair value based on the best
information available. Estimated fair value is generally based on either appraised value or measured by discounting estimated future
cash flows. Considerable management judgment is necessary to estimate discounted future cash flows. Accordingly, actual results could
vary significantly from such estimates.
Fair
Value Measurements
In
accordance with ASC 820, “Fair Value Measurements and Disclosures,” the Company applies fair value accounting for
all financial assets and liabilities and non-financial assets and liabilities that are recognized or disclosed at fair value in the financial
statements on a recurring basis. Fair value is defined as the price that would be received from selling an asset or paid to transfer
a liability in an orderly transaction between market participants at the measurement date. When determining the fair value measurements
for assets and liabilities which are required to be recorded at fair value, the Company considers the principal or most advantageous
market in which it would transact and the market-based risk measurements or assumptions that market participants would use in pricing
the asset or liability, such as risks inherent in valuation techniques, transfer restrictions and credit risk. Fair value is estimated
by applying the following hierarchy, which prioritizes the inputs used to measure fair value into three levels and bases the categorization
within the hierarchy upon the lowest level of input that is available and significant to the fair value measurement:
|
● |
Level 1 applies to assets
or liabilities for which there are quoted prices in active markets for identical assets or liabilities that we have the ability to
access at the measurement date. |
|
|
|
|
● |
Level 2 applies to assets
or liabilities for which there are inputs other than quoted prices included in Level 1 that are observable for the asset or liability,
either directly or indirectly, such as quoted prices for similar assets or liabilities in active markets; or quoted prices for identical
assets or liabilities in markets with insufficient volume or infrequent transactions (less active markets). |
|
|
|
|
● |
Level 3 applies to assets
or liabilities for which fair value is derived from valuation techniques in which one or more significant inputs are unobservable,
including our own assumptions. |
Derivative
Financial Instruments and Fair Value, Including ASU 2017-11 and ASU 2021-04
In
July 2017, the FASB issued ASU 2017-11 “Earnings Per Share (Topic 260) Distinguishing Liabilities from Equity (Topic 480) Derivatives
and Hedging (Topic 815).” The amendments in Part I of this Update change the classification analysis of certain equity-linked financial
instruments (or embedded features) with down round features. When determining whether certain financial instruments should be classified
as liabilities or equity instruments, a down round feature no longer precludes equity classification when assessing whether the instrument
is indexed to an entity’s own stock. The amendments also clarify existing disclosure requirements for equity-classified instruments.
As a result, a freestanding equity-linked financial instrument (or embedded conversion option) no longer would be accounted for as a
derivative liability at fair value as a result of the existence of a down round feature. For freestanding equity classified financial
instruments, the amendments require entities that present earnings (loss) per share (EPS) in accordance with Topic 260 to recognize the
effect of the down round feature when it is triggered. That effect is treated as a dividend and as a reduction of income available to
common stockholders in basic EPS. Convertible instruments with embedded conversion options that have down round features are now subject
to the specialized guidance for contingent beneficial conversion features (in Subtopic 470-20, Debt—Debt with Conversion and Other
Options), including related EPS guidance (in Topic 260).
In
May 2021, the FASB issued ASU 2021-04, Earnings Per Share (Topic 260), Debt—Modifications and Extinguishments (Subtopic 470-50),
Compensation—Stock Compensation (Topic 718), and Derivatives and Hedging—Contracts in Entity’s Own Equity (Subtopic
815-40), Issuer’s Accounting for Certain Modifications or Exchanges of Freestanding Equity-Classified Written Call Options. The
FASB issued this update to clarify and reduce diversity in an issuer’s accounting for modifications or exchanges of freestanding
equity-classified written call options (for example, warrants) that remain equity classified after modification or exchange. The guidance
clarifies whether an issuer should account for a modification or an exchange of a freestanding equity-classified written call option
that remains equity classified after modification or exchange as (1) an adjustment to equity (that is, deemed dividends) and, if so,
the related earnings per share (EPS) effects, if any, or (2) an expense and, if so, the manner and pattern of recognition. We adopted
this new accounting guidance on January 1, 2022. Under the new guidance, the FASB decided not to include convertible debt instruments
in the guidance because ASU No 2016-01, Financial Instruments – Overall (Subtopic 825-10) requires that an entity capture
the impact of changes in down round provision features of convertible debt within the fair value of the instruments.
Year
ended December 31, 2022 compared to the year ended December 31, 2021
The
following table summarizes the results of our consolidated continuing operations for the years ended December 31, 2022 and 2021:
| |
Year Ended December 31, | |
| |
2022 | | |
2021 | |
| |
| | |
% | | |
| | |
% | |
Net revenues | |
$ | 13,036,172 | | |
| 100.0 | % | |
$ | 3,223,896 | | |
| 100.0 | % |
Operating expenses: | |
| | | |
| | | |
| | | |
| | |
Direct costs of revenues | |
| 6,767,921 | | |
| 51.9 | % | |
| 5,292,430 | | |
| 164.2 | % |
General and administrative expenses | |
| 7,208,414 | | |
| 55.3 | % | |
| 7,507,613 | | |
| 232.9 | % |
Asset impairment | |
| - | | |
| 0.0 | % | |
| 2,300,826 | | |
| 71.4 | % |
Depreciation and amortization | |
| 469,371 | | |
| 3.6 | % | |
| 643,551 | | |
| 20.0 | % |
Loss from continuing operations before other income (expense) and income taxes | |
| (1,409,534 | ) | |
| -10.8 | % | |
| (12,520,524 | ) | |
| -388.4 | % |
Other income, net | |
| 499,681 | | |
| 3.8 | % | |
| 5,376,244 | | |
| 166.8 | % |
Gain from forgiveness of debt | |
| 334,819 | | |
| 2.6 | % | |
| 1,985,121 | | |
| 61.6 | % |
(Loss) gain from legal settlements, net | |
| (129,153 | ) | |
| -1.0 | % | |
| 3,252,144 | | |
| 100.9 | % |
Interest expense | |
| (2,257,544 | ) | |
| -17.3 | % | |
| (3,185,828 | ) | |
| -98.8 | % |
Provision for income taxes | |
| (312,849 | ) | |
| -2.4 | % | |
| (179,530 | ) | |
| -5.6 | % |
Net loss from continuing operations | |
$ | (3,274,580 | ) | |
| -25.1 | % | |
$ | (5,272,373 | ) | |
| -163.5 | % |
Net
Revenues
Net
revenues were $13.0 million for the year ended December 31, 2022, as compared to $3.2 million for the year ended December 31, 2021, an
increase of $9.8 million. We attribute the increase in net revenues primarily due to retroactive and current billings and collections
and increased inpatient admissions at our Big South Fork Medical Center. We began billing as a Critical Access Hospital in the three
months ended June 30, 2022 retroactive to July 1, 2021.
Direct
Costs of Revenues
Direct costs of revenues increased by $1.5 million
for the year ended December 31, 2022 compared to 2021. We attribute the increase in 2022 primarily to higher professional fees and salaries
and wages, partially offset by lower costs at Jellico due to the lease termination in March 2021. Professional fees increased due to greater
inpatient admissions and to the restructuring of our relationships with certain professional service firms. Salaries and wages increased
due to greater inpatient admissions, increased non-clinical staffing and reduced contract labor.
General and Administrative Expenses
General and administrative expenses
decreased by $0.3 million, or 4.0%, in the year ended December 31, 2022 compared to 2021. We attribute the decrease to reductions of
general and administrative expenses at Jellico Community Hospital and Jamestown Regional Medical Center. While Jamestown Regional
Medical Center was closed in 2019, certain fixed expenses remain. These decreases were partially offset by increases in general and
administrative expenses at Big South Fork Medical Center, as well as corporate related expenses.
Asset
Impairment
We
recorded an asset impairment charge of $2.3 million as of December 31, 2021 for Jamestown Regional Medical Center’s building. In
determining the fair value of Jamestown Regional Medical Center’s building, the impairment reflected the changed condition of the
building that has not been in use since operations were suspended in June 2019.
Depreciation
and Amortization Expenses
Depreciation
and amortization expenses were $0.5 million for the year ended December 31, 2022 as compared to $0.6 million in the year ended December
31, 2021. We attribute the decrease to fully depreciating certain assets in 2021. In addition, we recorded a $2.3 million impairment
of Jamestown Regional Medical Center’s building in the fourth quarter of 2021, which resulted in a reduction of depreciation and
amortization for the building for the year ended December 31, 2022.
Loss
from Continuing Operations Before Other Income (Expense) and Income Taxes
Our
loss from continuing operations before other income (expense) and income taxes for the year ended December 31, 2022 was $1.4 million
compared to a loss of $12.5 million for the year ended December 31, 2021. We attribute the decrease in the operating loss primarily to
the increase in net revenues, the asset impairment charge in 2021 as well as the reduction in general and administrative expenses.
Other
Income, Net
Other
income, net of $0.5 million for the year ended December 31, 2022 consisted primarily of adjustments totaling approximately $0.3 million
for certain previously accrued payroll related expenses, $0.2 million of non-cash interest income associated with the note receivable
from related party, $0.6 million of income from HHS Provider Relief Funds and $0.6 million of various other income items, net, partially
offset by $1.2 million of penalties and interest associated with past due payroll taxes. Other income, net of $5.4 million for the year
ended December 31, 2021 consisted primarily of $4.4 million of income from HHS Provider Relief Funds and $1.5 million of income from
employee retention federal tax credits, partially offset by $0.4 million in penalties associated with non-payment of payroll taxes and
$0.3 million of loss on disposal of equipment and inventory.
Gain
from Forgiveness of Debt
We
had gains of $0.3 million and $2.0 million from the forgiveness of PPP Notes in the years ended December 31, 2022 and 2021, respectively.
(Loss)
Gain from Legal Settlements, Net
The
(loss) gain from legal settlements, net was ($0.1) million and $3.3 million for the years ended December 31, 2022 and 2021, respectively.
The gain from legal settlements, net of $3.3 million for 2021 resulted primarily from: (i) a gain of $0.6 million from the settlements
of obligations under accounts receivable sale agreements; (ii) a gain of $2.2 million from the settlement of obligations under a debenture;
and (iii) a gain of $0.3 million pursuant to the settlement of obligations owed under professional services agreements.
Interest
Expense
Interest
expense for the year ended December 31, 2022 was $2.3 million compared to $3.2 million in 2021. Interest expense for the year ended December
31, 2022 included $2.2 million for interest on debentures and notes payable and $0.1 million for interest on loans from Mr. Diamantis,
a former member of our Board of Directors. Interest expense for the year ended December 31, 2021 included $3.1 million for interest on
debentures and notes payable and $0.1 million for interest on loans from Mr. Diamantis. The decrease in interest expense in the year
ended December 31, 2022 compared to 2021 was due primarily to the exchange of debentures and notes payable in November 2021 for preferred
stock.
Provision
for Income Taxes
We
incurred an income tax provision of $0.3 million and $0.2 million for the years ended December 31, 2022 and 2021, respectively, for
federal and state income taxes.
Net
Loss from Continuing Operations
The
net loss from continuing operations for the year ended December 31, 2022 was $3.3 million compared to a net loss from continuing
operations of $5.3 million for the year ended December 31, 2021. The decrease in the net loss in 2022 as compared to 2021 of
approximately $2.3 million was primarily due to the decrease in the loss from continuing operations before other income (expense)
and income taxes of $11.1 million and a reduction in interest expense of $0.9 million, partially offset by the income from HHS Provider Relief
Funds of $0.6 million in 2022 compared to a gain of $4.4 million in 2021, a loss from legal settlements, net of $0.1 million in 2022
compared to a gain of $3.3 million in 2021, a gain on forgiveness of PPP Notes of $0.3 million in the year ended December 31,
2022 compared to a $2.0 million gain in 2021 and an increase in the provision for income taxes of $0.1 million in 2022 compared to 2021.
Liquidity
and Capital Resources
Overview
For
the years ended December 31, 2022 and 2021, we financed our operations from issuances of preferred stock, debentures and notes payable
and loans from Mr. Diamantis, a former member of our Board of Directors. Also, during the years ended December 31, 2022 and 2021, we
received $0.3 million and $0.9 million, respectively, from HHS Provider Relief Funds. The HHS Provider Relief Funds are grants, not loans,
and HHS will not require repayment, but providers are restricted and the funds must be used only for grant approved purposes as more
fully discussed in Note 1 to the consolidated financial statements incorporated by reference in this prospectus.
During the year ended December 31, 2022, we received $1.5 million from the issuance of our Series P Convertible Redeemable Preferred
Stock (“Series P Preferred Stock”) and we received cash of $0.5 million from the issuance of debentures. In the year ended
December 31, 2021, we received cash of $9.0 million from issuances of our Series O Convertible Redeemable Preferred Stock (“Series
O Preferred Stock”) and we received cash of $1.2 million from the issuances of promissory notes. During the year ended December
31, 2022, Mr. Diamantis loaned the Company $1.1 million, which was used to repay a portion of the amounts due under a third-party promissory
note, pursuant to a personal guaranty of the promissory note by Mr. Diamantis. During the year ended December 31, 2021, Mr. Diamantis
loaned the Company $0.9 million, the majority of which was used for working capital purposes. During the years ended December 31, 2022
and 2021, the Company repaid Mr. Diamantis $0.2 million and $0.9 million, respectively. During the year ended December 31, 2021, we received
$1.5 million in federal employee retention credits, which we applied to outstanding past-due payroll taxes.
On
November 7, 2021, we entered into Exchange and Amendment Agreements (the “November 2021 Exchange Agreements”) with certain
institutional investors in the Company. In the November 2021 Exchange Agreements, the investors agreed to reduce their holdings of $1.1
million principal value of then outstanding warrant promissory notes payable and $4.5 million of then outstanding non-convertible debentures,
plus accrued interest thereon of approximately $1.5 million, by exchanging the indebtedness and accrued interest for 8,544.870 shares
of the Company’s Series P Preferred Stock with a stated value of $8,544,870. After the November 2021 Exchange Agreements, the investors
continued to own approximately $8.2 million of the then outstanding debentures, plus the associated accrued interest of approximately
$5.1 million at December 31, 2022. In addition, pursuant to the November 2021 Exchange Agreements, the expiration dates of the certain
warrants that were issued by the Company to the investors in March 2017, as more fully described in Note 12 to the consolidated financial
statements incorporated by reference in this prospectus, were extended from March 21, 2022 to March 21, 2024.
On
June 25, 2021, the Company sold HTS and AMSG to InnovaQor and the Company received 14,950 shares of InnovaQor’s Series B-1 Preferred
Stock with a stated value of $1,000 per share and valued at $9.1 million as consideration for the sale. In addition, $2.2 million of
net liabilities of HTS and AMSG were transferred to InnovaQor. The sale is more fully discussed above under the heading, “Discontinued
Operations,” and in Note 15 to our consolidated financial statements incorporated by reference in this prospectus.
Future
cash needs for working capital, capital expenditures, pursuit of opportunities in the behavioral sector, debt service obligations and
potential acquisitions will require management to seek additional capital. The Company and our facilities may also receive additional
government assistance. The sale/issuance of additional equity will result in additional dilution to our stockholders.
Each
of these financing transactions is more fully discussed in the footnotes to our consolidated financial statements incorporated by
reference in this prospectus.
Going
Concern and Liquidity
Under
ASU 2014-15, Presentation of Financial Statements—Going Concern (Subtopic 205-40) (“ASC 205-40”), the Company
has the responsibility to evaluate whether conditions and/or events raise substantial doubt about its ability to meet its future financial
obligations as they become due within one year after the date that the financial statements are issued. As required by ASC 205-40, this
evaluation shall initially not take into consideration the potential mitigating effects of plans that have not been fully implemented
as of the date the financial statements are issued. Management has assessed the Company’s ability to continue as a going concern
in accordance with the requirement of ASC 205-40.
As reflected in the consolidated financial
statements incorporated by reference in this prospectus, the Company had a working capital deficit and a stockholders’ deficit
of $42.9 million and $29.1 million, respectively, at December 31, 2022. The Company had a loss from continuing operations of approximately
$3.3 million and $5.3 million for the years ended December 31, 2022 and 2021, respectively, and cash used in its operating activities
was $0.2 million and $8.9 million for the years ended December 31, 2022 and 2021, respectively. As of the date of this prospectus,
our cash is deficient and payments for our operations in the ordinary course are not being made. The continued losses and other related
factors, including past due accounts payable and payroll taxes as well as payment defaults under the terms of certain outstanding notes
payable and debentures, as more fully discussed in Notes 1, 7 and 8 to the consolidated financial statements incorporated by reference
in this prospectus, raise substantial doubt about the Company’s ability to continue as a going concern for 12 months from the
filing date of the financial statements.
The
Company’s consolidated financial statements incorporated by reference in this prospectus are prepared assuming the Company
can continue as a going concern, which contemplates continuity of operations through realization of assets, and the settling of liabilities
in the normal course of business. As more fully discussed above and in Note 15 to the consolidated financial statements incorporated
by reference in this prospectus, on June 25, 2021, the Company sold HTS and AMSG to InnovaQor and the Company received 14,950 shares
of InnovaQor’s Series B-1 Preferred Stock valued at $9.1 million as consideration for the sale. In addition, $2.2 million of net
liabilities of HTS and AMSG were transferred to InnovaQor. The Company has reflected the assets and liabilities relating to HTS and AMSG
held prior to the sale as part of discontinued operations.
We need to raise additional funds until we begin
to realize positive cash flow from operations. There can be no assurance that we will be able to achieve our business plan, which is
to acquire and operate clusters of rural hospitals and related service providers, raise any additional capital or secure the additional
financing necessary to implement our current operating plan. Our ability to continue as a going concern is dependent upon our ability
to significantly increase our revenues, reduce our operating costs and eventually achieve profitable operations. The consolidated financial
statements incorporated by reference in this prospectus do not include any adjustments that might be necessary if we are unable
to continue as a going concern.
The
following table presents our capital resources as of December 31, 2022 and 2021:
| |
December 31, | | |
December 31, | | |
| |
| |
2022 | | |
2021 | | |
Change | |
| |
| | |
| | |
| |
Cash | |
$ | 499,470 | | |
$ | 724,524 | | |
$ | (225,054 | ) |
Working capital deficit | |
| (42,944,995 | ) | |
| (41,641,960 | ) | |
| (1,303,035 | ) |
Total debt | |
| 14,534,630 | | |
| 15,017,059 | | |
| (482,429 | ) |
Finance lease obligation | |
| 220,461 | | |
| 220,461 | | |
| - | |
Stockholders’ deficit | |
| (29,094,588 | ) | |
| (27,301,524 | ) | |
| (1,793,064 | ) |
The
following table presents the major sources and uses of cash for the years ended December 31, 2022 and 2021:
| |
Year Ended December 31, | | |
| |
| |
2022 | | |
2021 | | |
Change | |
| |
| | |
| | |
| |
Net cash used in operations | |
$ | (218,348 | ) | |
$ | (8,912,682 | ) | |
$ | 8,694,334 | |
Net cash used in investing activities | |
| (905,191 | ) | |
| (374,473 | ) | |
| (530,718 | ) |
Net cash provided by financing activities | |
| 898,485 | | |
| 9,986,326 | | |
| (9,087,841 | ) |
| |
| | | |
| | | |
| | |
Net change in cash | |
| (225,054 | ) | |
| 699,171 | | |
| (924,225 | ) |
Cash and cash equivalents, beginning of the year | |
| 724,524 | | |
| 25,353 | | |
| 699,171 | |
Cash and cash equivalents, end of the period | |
$ | 499,470 | | |
$ | 724,524 | | |
$ | (225,054 | ) |
The
components of cash used in operations for the years ended December 31, 2022 and 2021 are presented in the following
table:
| |
Year Ended December 31, | | |
| |
| |
2022 | | |
2021 | | |
Change | |
| |
| | |
| | |
| |
Net loss from continuing operations | |
$ | (3,274,580 | ) | |
$ | (5,272,373 | ) | |
$ | 1,997,793 | |
Non-cash adjustments to net loss (1) | |
| (511,631 | ) | |
| (8,192,389 | ) | |
| 7,680,758 | |
Changes in operating assets and liabilities: | |
| | | |
| | | |
| | |
Accounts receivable | |
| (343,446 | ) | |
| (544,616 | ) | |
| 201,170 | |
Inventory | |
| 37,868 | | |
| 164,902 | | |
| (127,034 | ) |
Accounts payable and accrued expenses | |
| 3,625,158 | | |
| 4,540,724 | | |
| (915,566 | ) |
Income tax assets and liabilities | |
| 312,849 | | |
| 179,530 | | |
| 133,319 | |
Other | |
| (71,202 | ) | |
| 102,450 | | |
| (173,652 | ) |
Net cash used in operating activities of continuing operations | |
| (224,984 | ) | |
| (9,021,772 | ) | |
| 8,796,788 | |
Net cash provided by operating
activities of discontinued operations | |
| 6,636 | | |
| 109,090 | | |
| (102,454 | ) |
Net cash used in operations | |
$ | (218,348 | ) | |
$ | (8,912,682 | ) | |
$ | 8,694,334 | |
(1) |
Non-cash
adjustments to net loss from continuing operations for the year ended December 31, 2022 of $0.5 million include primarily $0.3
million of other income from forgiveness of PPP Notes, $0.6 million of income from HHS Provider Relief Funds and $0.2 million of
non-cash interest income, partially offset by $0.1 million of loss from legal settlements, net, and $0.5 million of depreciation and
amortization. Non-cash adjustments to net loss from continuing operations for the year ended December 31, 2021 of $8.2 million
include primarily an $11.3 million gain from the sale of HTS and AMSG, $3.3 million gain from legal settlements, $2.0 million gain
from extinguishment of debt, $4.4 million gain from HHS provider relief funds and $1.5 million of income from employee retention
credits, partially offset by net income from discontinued operations of $10.9 million, $2.3 million of fixed asset impairment and
$0.6 million of depreciation and amortization. |
Cash
of $0.9 million was used in investing activities during the year ended December 31, 2022, of which $35,230 was used to purchase equipment and $0.9 million was used to fund working capital needs at InnovaQor (classified as a note receivable / receivable from related party).
Cash of $0.4 million was used in the year ended December 31, 2021 to fund working capital needs at InnovaQor (classified as receivable
from related party).
Cash
provided by financing activities for the year ended December 31, 2022 of $0.9 million included $1.1 million in loans from a former member
of our Board of Directors, $0.5 million from the issuance of debentures, $1.5 million from the issuance of shares of our Series P Preferred
Stock and $0.3 million in HHS Provider Relief funds, partially offset by $0.2 million in payments of loans from a former member of our
Board of Directors, $1.4 million in payments of notes payable, $150,000 in payments of debentures and $0.7 million in payments of accounts
receivable under sales agreements. Cash provided by financing activities for the year ended December 31, 2021 of $10.0 million included
primarily $9.0 million in proceeds from the issuance of our Series O Preferred Stock, $0.9 million in loans from a former member of our
Board of Directors, $0.9 million from HHS Provider Relief Funds and $1.2 million from the issuances of notes payable, partially offset
by $0.9 million in payments of loans from a former member of our Board of Directors, $0.7 million in payments of notes payable and $0.5
million in payments of accounts receivable under sales agreements.
Common
Stock and Common Stock Equivalents
The
Company had 29.1 billion and 4.2 million shares of its common stock issued and outstanding at December 31, 2022 and December 31,
2021, respectively. During the year ended December 31, 2022, the Company issued one share of its common stock upon conversion of
1,750,000 shares of its Series F Convertible Preferred Stock, 16.0 billion shares of its common stock upon conversions of $3.0
million of stated value of its Series N Convertible Redeemable Preferred Stock and 13.1 billion shares of its common stock upon the
conversions of $1.2 million of stated value of its Series O Preferred Stock. During the year ended December 31, 2021, the Company
issued 9,500 shares of its common stock upon the exchange and conversions of $1.2 million of stated value of its Series M
Convertible Redeemable Preferred Stock the (“Series M Preferred Stock”) and 4.2 million shares of its common stock
upon the conversions of $23.5 million of stated value of its Series N Preferred Stock.
The
terms of certain of the outstanding warrants, convertible preferred stock and convertible debentures issued by the Company provide for
reductions in the per share exercise prices of the warrants and the per share conversion prices of the debentures and preferred stock
(if applicable and subject to a floor in certain cases), in the event that the Company issues common stock or common stock equivalents
(as that term is defined in the agreements) at an effective exercise/conversion price that is less than the then exercise/conversion
price of the outstanding warrants, preferred stock or debentures, as the case may be. In addition, the majority of these equity-based
securities contain exercise/conversion prices that vary based upon the price of the Company’s common stock on the date of exercise/conversion
(see Notes 8, 11 and 12 to the consolidated financial statements incorporated by reference in this prospectus). These provisions
have resulted in significant dilution of the Company’s common stock and have given rise to reverse splits of the Company’s
common stock, including a 1-for-1,000 reverse stock split effected on July 16, 2021 and a 1-for-10,000 reverse stock split effected on
March 15, 2022. As a result of these down round provisions, the potential common stock equivalents, including outstanding common stock,
totaled 1.0 trillion at December 31, 2022 and 1.0 trillion at March 30, 2023.
On
August 13, 2020, Mr. Diamantis entered into the Voting Agreement with the Company, Mr. Seamus Lagan and Alcimede LLC (of which Mr. Lagan,
the Company’s Chief Executive Officer, is the sole manager) pursuant to which Mr. Diamantis granted an irrevocable proxy to Mr.
Lagan to vote the Series M Preferred Stock held by Mr. Diamantis. Mr. Diamantis has retained all other rights under the Series M Preferred
Stock. Regardless of the number of shares of Series M Preferred Stock outstanding and so long as at least one share of Series M Preferred
Stock is outstanding, the outstanding shares of Series M Preferred Stock shall have the number of votes, in the aggregate, equal to 51%
of all votes entitled to be voted at any meeting of stockholders or action by written consent. This means that the holders of Series
M Preferred Stock have sufficient votes, by themselves, to approve or defeat any proposal voted on by the Company’s stockholders,
unless there is a supermajority required under applicable law or by agreement.
Also,
on November 5, 2021, the Company amended its Certificate of Incorporation, as amended, to provide that the number of authorized shares
of its common stock or preferred stock may be increased or decreased (but not below the number of shares then outstanding) by the affirmative
vote of the holders of a majority in voting power of the stock of the Company entitled to vote generally in the election of directors,
irrespective of the provisions of Section 242(b)(2) of the General Corporation Law of the State of Delaware (or any successor provision
thereto), voting together as a single class, without a separate vote of the holders of the class or classes the number of authorized
shares of which are being increased or decreased unless a vote by any holders of one or more series of preferred stock is required by
the express terms of any series of preferred stock pursuant to the terms thereof.
As
a result of the Voting Agreement and the November 5, 2021 amendment to the Company’s Certificate of Incorporation discussed above,
as of the date of this prospectus, the Company believes that it has the ability to ensure that it has and or can obtain sufficient
authorized shares of its common stock to cover all potentially dilutive shares of common stock outstanding.
Inflation
and Supply Chain Issues
The
healthcare industry is very labor intensive and salaries and benefits are subject to inflationary pressures, as are supply and other
costs. The nationwide shortage of nurses and other clinical staff and support personnel has been a significant operating issue facing
us and other healthcare providers. In particular, like others in the healthcare industry, we continue to experience a shortage of nurses
and other clinical staff and support personnel, which has been exacerbated by the COVID-19 pandemic. We are treating patients with COVID-19
in our facilities and, in some areas, the increased demand for care is putting a strain on our resources and staff, which has required
us to utilize higher-cost temporary labor and pay premiums above standard compensation for essential workers. The length and extent of
the disruptions caused by the COVID-19 pandemic are currently unknown; however, we expect such disruptions to continue. This staffing
shortage may require us to further enhance wages and benefits to recruit and retain nurses and other clinical staff and support personnel
or require us to hire expensive temporary personnel. Our ability to pass on increased costs associated with providing healthcare to Medicare
and Medicaid patients is limited due to various federal, state and local laws which have been enacted that, in certain cases, limit our
ability to increase prices.
MANAGEMENT
Executive
Officers and Directors
The
following table sets forth information with respect to persons who are currently serving as directors and executive officers of the Company.
Name |
|
Age |
|
Positions |
Seamus Lagan |
|
53 |
|
President, Chief Executive Officer, Interim Chief Financial
Officer and Director |
Gary L. Blum |
|
82 |
|
Director |
Trevor Langley |
|
60 |
|
Director |
All
directors of the Company serve one-year terms and hold office until the next annual meeting of stockholders and until their respective
successors are duly elected and qualified.
Executive
Officers’ and Directors’ Biographies
Seamus
Lagan was appointed Chief Executive Officer and President and a director of the Company on November 2, 2015 and as Chief Executive
Officer and a director of Medytox Solutions, Inc., a wholly-owned subsidiary of the Company (“Medytox”), effective September
15, 2014. Mr. Lagan served as Interim Chief Financial Officer of the Company from September 30, 2016 through May 24, 2017. He was again
appointed Interim Chief Financial Officer effective October 13, 2017, and served through April 8, 2019. Mr. Lagan has also been the Interim
Chief Financial Officer of the Company since May 10, 2019. Mr. Lagan has been, either individually or through Alcimede LLC or Alcimede
Limited, a consultant to Medytox since May 2011. Mr. Lagan has been a manager of Alcimede LLC since its formation in 2007. Alcimede LLC
is a privately-held, Delaware limited liability company which provides various consulting services, including management, organization,
and financial consulting services. Alcimede Limited is a Bahamas company that provides similar consulting services as Alcimede LLC. Mr.
Lagan also currently serves, through Alcimede Limited, as chief executive officer of most of the subsidiaries of the Company. From September
2008 through May 2011, Mr. Lagan was a private investor. Mr. Lagan graduated from Ballymena Technical College in Ireland in 1989.
Gary
L. Blum has served as a director of the Company since October 11, 2017. He established the Law Offices of Gary L. Blum in 1986. Mr.
Blum has served as counsel for a wide variety of closely-held and public companies for over three decades. Prior to becoming an attorney,
he was a tenured professor of philosophy at the University of Nebraska, Omaha. From September 2009 to July 2017, Mr. Blum served as Chairman,
Chief Executive Officer and Chief Financial Officer of Thunderclap Entertainment, Inc. (now known as TraqIQ, Inc.), a company whose business
was to develop, produce and distribute low-budget independent feature films. He has also been Chairman of Diamond Wellness Holdings,
Inc. (formerly PotNetwork Holdings, Inc.) since November 2015 and was its Chief Executive Officer from November 2015 until
September 2017. That company is engaged in the development and sales of hemp-derived CBD oil containing products.
Trevor
Langley has served as a director of the Company since April 9, 2017. Since 2006, he has been the Owner and Managing Partner of Avanti
Capital Group LLC/Avanti Partners, LLC (“Avanti”). Avanti assists micro, small and mid-cap publicly traded companies and
those looking to become public by leveraging traditional and new communication technologies with a specialization in healthcare and alternative-energy
markets. Avanti also provides comprehensive consulting services.
Family
Relationships amongst Directors and Executive Officers
There
are no family relationships between the executive officers and directors.
Audit
Committee and Audit Committee Financial Expert
The
purpose of the audit committee is to review the Company’s audited financial statements with management, review the performance
of the Company’s independent registered public accountants, approve audit fees and fees for the preparation of the Company’s
tax returns, review the Company’s internal accounting policies and internal control procedures and consider and appoint the Company’s
independent registered public accountants. The audit committee has the authority to engage the services of outside experts and advisors
as it deems necessary or appropriate to carry out its duties and responsibilities.
The
audit committee charter is available on the Company’s website at www.rennovahealth.com by selecting “Investors”
and then “Corporate Governance” from the available options.
The
audit committee of the Company consists of Trevor Langley and Gary L. Blum. Each member of the audit committee qualifies as “independent”
for purposes of membership on audit committees pursuant to the rules and regulations of the SEC. In addition, the Board of Directors
of the Company has determined that Trevor Langley qualifies as an “audit committee financial expert” as defined by the rules
and regulations of the SEC.
Code
of Conduct
The
Company has adopted a written code of conduct (the “Code”), which is applicable to the Board of Directors and officers of
the Company, including, but not limited to the Company’s Chief Executive Officer, Chief Financial Officer, Controller and all persons
performing similar functions to the foregoing officers of the Company. We intend to post amendments to or waivers from the Code (to the
extent applicable to our Principal Executive Officer, Principal Financial Officer, Principal Accounting Officer or Controller, or persons
performing similar functions) on our website at www.rennovahealth.com. A copy of the Code will be provided to any person free of charge
upon request by writing to Rennova Health, Inc., Attention: Secretary, 400 South Australian Avenue, Suite 800, West Palm Beach, Florida
33401.
Risk
Management
The
board of directors, as a whole, monitors and considers policies to manage risk as part of its regular activities. The audit committee
is primarily responsible for the identification and review of financial risk and reports its activities to the board of directors.
Director
Independence
The
board of directors has affirmatively determined that each of Gary L. Blum and Trevor Langley is an “independent director”.
No director qualifies as independent unless the board of directors affirmatively determines that the director does not have a material
relationship with the listed company that would interfere with the exercise of independent judgment.
EXECUTIVE
COMPENSATION
The
following table sets forth all of the compensation awarded to, earned by or paid to each individual that served as our principal executive
officer or principal financial officer during the fiscal years ended December 31, 2022 and 2021. The Company did not have
any other executive officers during the fiscal years ended December 31, 2022 and 2021.
SUMMARY
COMPENSATION TABLE
Name and Principal Position | |
Fiscal Year | | |
Salary | | |
Stock Awards | | |
Option Awards | | |
Nonequity Incentive Plan Compensation | | |
Nonqualified Deferred Compensation Earnings | | |
All Other Compensation (2) | | |
Total | |
| |
| | |
| | |
| | |
| | |
| | |
| | |
| | |
| |
Seamus Lagan | |
| 2022 | (1) | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 424,500 | | |
$ | 424,500 | |
President, CEO, Interim CFO and Director | |
| 2021 | (1) | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 387,000 | | |
$ | 387,000 | |
(1) |
Mr. Lagan was Interim Chief
Financial Officer of the Company from September 30, 2016 through May 24, 2017. He was again appointed Interim Chief Financial Officer
effective October 13, 2017, and served through June 30, 2018. Mr. Lagan has also been the Interim Chief Financial officer of the
Company since May 10, 2019. |
|
|
(2) |
All
other compensation for the year ended December 31, 2022 includes, for Mr. Lagan, consulting fees of $375,000, an incentive
bonus of $37,500 and an automobile expense allowance of $12,000. All other compensation for the year ended December 31, 2021
includes, for Mr. Lagan, consulting fees of $375,000 and an automobile expense allowance of $12,000. |
OUTSTANDING
EQUITY AWARDS AT FISCAL YEAR-END
The
following table provides information regarding outstanding equity awards held by the named executive officers at December 31, 2022:
Name | |
Number of
shares
underlying
unexercised
options
exercisable | | |
Number of
shares
underlying
unexercised
options
unexercisable | | |
Equity
Incentive
Plan
Awards;
Number of
shares
underlying
unexercised
unearned
options | | |
Option
exercise
price | | |
Option
Expiration
date | |
Number
of
shares
or units
of stock
that
have
not
vested | | |
Market
value
of
shares
or
units
of
stock
that
have
not
vested $ | | |
Equity
Incentive
Plan
Awards:
Number
of
unearned
shares,
units or
other
rights
that have
not
vested | | |
Equity
Incentive
Plan
Awards:
Market
or
payout
value of
unearned
shares,
units or
other
rights
that have
not
vested $ | |
Seamus Lagan | |
| 1 | | |
| - | | |
| - | | |
$ | 10,000,000 | | |
3/23/2026 | |
| - | | |
| - | | |
| - | | |
| - | |
| |
| 1 | | |
| - | | |
| - | | |
$ | 5,000,000 | | |
3/23/2026 | |
| - | | |
| - | | |
| - | | |
| - | |
| |
| 1 | | |
| - | | |
| - | | |
$ | 250,000 | | |
5/2/2026 | |
| - | | |
| - | | |
| - | | |
| - | |
| |
| 1 | | |
| - | | |
| - | | |
$ | 75,000 | | |
7/17/2026 | |
| - | | |
| - | | |
| - | | |
| - | |
AGREEMENTS
WITH NAMED EXECUTIVE OFFICERS
Seamus
Lagan
On
October 1, 2012, Medytox Solutions, Inc. (“Medytox”) entered into a consulting agreement with Alcimede LLC, which is controlled
by Mr. Lagan. This agreement replaced and superseded a previous Alcimede consulting agreement. This agreement was originally for three
years, and was then subject to annual renewals thereafter, unless either party gave notice of non-renewal. The agreement provided for
a retainer of $20,000 per month and reimbursement to Alcimede for its out of pocket expenses. The parties agreed to cancel the options
issued pursuant to the prior agreement. Under the new agreement, Alcimede was issued 4,500,000 shares of common stock of Medytox and
1,000 shares of Series B Preferred Stock of Medytox. In addition, Alcimede received options to purchase (i) 1,000,000 shares of common
stock of Medytox exercisable at $2.50 per share through December 31, 2017, (ii) 1,000,000 shares of common stock of Medytox exercisable
at $5.00 per share through December 31, 2017 and (iii) 1,000,000 shares of common stock of Medytox exercisable at $10.00 a share through
December 31, 2022. On June 29, 2015, Alcimede exercised the option to purchase 1,000,000 shares of common stock of Medytox at an exercise
price of $2.50 per share. The parties agreed to cancel the remaining options to purchase 1,000,000 shares of common stock of Medytox
at an exercise price of $5.00 per share and 1,000,000 shares of common stock at an exercise price of $10.00 per share in connection with
the merger of Medytox with the Company on November 2, 2015. The share amounts and exercise prices in this paragraph are on a pre-merger
basis and do not reflect the reverse splits effected by the Company since the merger.
Effective
September 11, 2014 and in conjunction with the appointment of Mr. Lagan as our Chief Executive Officer, such consulting agreement with
Alcimede was amended to provide for a monthly retainer of $31,250, and we agreed to provide Mr. Lagan with an automobile. During the
year ended December 31, 2016, Alcimede received a cash bonus of $200,000. On April 1, 2017, Alcimede agreed to a voluntary reduction
in the monthly retainer to $20,833, which was increased back up to $31,250 in April 2018. In September 2020, it was agreed to pay $100,000
to renew the Alcimede consulting agreement for a three-year period. It was further agreed that this consulting agreement could be assigned
to another entity and that termination of the agreement would trigger a $500,000 payment. On November 1, 2021, that consulting agreement
was replaced by an agreement between the Company and Alcimede Limited, a Bahamian company of which Mr. Lagan is the Managing Director.
The new agreement is for three years and is renewable for one-year periods thereafter. It contains similar terms as the prior agreement
with regard to monthly fees and expense reimbursements. Alcimede Limited received a $37,500 cash bonus during the year ended December
31, 2022.
Director
Compensation
Non-employee
directors receive an annual cash retainer of $40,000 and may be granted stock options. We do not pay employee directors for Board service
in addition to their regular employee compensation. The Board has the primary responsibility for considering and determining the amount
of director compensation.
The
following table shows amounts earned by each non-employee Director in the fiscal year ended December 31, 2022:
Director | |
Fees
earned
or paid
in cash | | |
Stock
Awards | | |
Option
Awards | | |
Non-equity
Incentive Plan
Compensation | | |
All
Other
Compensation | | |
Total | |
Gary L. Blum | |
$ | 40,008 | | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | 40,008 | |
Trevor Langley | |
$ | 40,008 | | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | - | | |
$ | 40,008 | |
In
December 2022, the Company’s two non-executive directors each agreed to a $50,000 cash payment in lieu of accrued director
fees of $115,042 for Mr. Blum and accrued director fees of $140,044 for Mr. Langley. Accordingly, no fees were owed to any director at December 31, 2022.
CERTAIN
RELATIONSHIPS AND RELATED PARTY TRANSACTIONS
Alcimede
Limited and Alcimede LLC, each of which is controlled by Mr. Lagan, billed the Company an aggregate of $0.4 million and Alcimede LLC
billed the Company $0.4 million for consulting fees and reimbursement of expenses pursuant to a consulting agreement for the years ended
December 31, 2021 and 2020, respectively. Alcimee Limited and Alcimede LLC billed the Company $0.3 million and $0.3 million, the nine
months ended September 30, 2022 and 2021, respectively. In addition, Alcimede LLC received a payment of $100,000 for the year ended December
31, 2020 for the renewal and amendment to the then existing contract. On April 2, 2017, Alcimede LLC agreed to a voluntary reduction
in the monthly retainer payable by the Company from $31,250 to $20,833, which was increased back up to $31,250 in April 2018. On February
3, 2015, the Company borrowed $3.0 million from Alcimede LLC. The note had an interest rate of 6% and was originally due on February
2, 2016. Alcimede LLC later agreed to extend the maturity date of the loan to August 2, 2017. On June 29, 2015, Alcimede LLC exercised
options granted in October 2012 to purchase shares of common stock, and the loan outstanding was reduced in satisfaction of the aggregate
exercise price of $2.5 million. In August 2016, $0.3 million was repaid by the Company through the issuance of shares of common stock.
In March 2017, the Company and Mr. Lagan agreed that a payment made to Alcimede LLC in the amount of $50,000 would be deducted from the
outstanding balance of the note. On August 2, 2017, the Company and Alcimede LLC agreed to further extend the maturity date of the loan
to August 2, 2018. On July 20, 2018, the Company filed a Certificate of Designation with the Secretary of State of the State of Delaware
to authorize the issuance of up to 250,000 shares of its Series J Convertible Preferred Stock (the “Series J Preferred Stock”).
On July 23, 2018, the Company entered into an Exchange Agreement (the “Series J Agreement”) with Alcimede LLC. Pursuant to
the Series J Agreement, the Company issued to Alcimede LLC 250,000 shares of the Series J Preferred Stock in exchange for the cancellation
of the outstanding principal and interest owed by the Company to Alcimede LLC under the Note, dated February 5, 2015, and the cancellation
of certain amounts owed by the Company to Alcimede LLC under the consulting agreement between the parties. The total amount of consideration
paid by Alcimede LLC to the Company equaled $250,000. Each share of the Series J Preferred Stock had a stated value of $1.00 and was
entitled to 8% per annum cumulative dividends at the discretion of the Company’s Board of Directors. On September 27, 2019, the
Company filed a Certificate of Designation with the Secretary of State of the State of Delaware to authorize the issuance of up to 250,000
shares of its Series K Convertible Preferred Stock (the “Series K Preferred Stock”). On December 29, 2019, the Company entered
into an Exchange Agreement (the “Series K Agreement”) with Alcimede LLC. Pursuant to the Series K Agreement, the Company
issued to Alcimede LLC 250,000 shares of the Series K Preferred Stock in exchange for the 250,000 shares of Series J Preferred Stock.
The shares of Series J Preferred Stock were cancelled and, under the Series K Agreement, Alcimede LLC relinquished all rights to any
cumulative dividends on the Series J Preferred Stock. The terms of the Series K Preferred Stock did not provide for cumulative dividends.
On May 4, 2020, the Company filed a Certificate of Designation with the Secretary of State of the State of Delaware to authorize the
issuance of up to 250,000 shares of Series L Convertible Preferred Stock (the “Series L Preferred Stock”). On May 5, 2020,
the Company entered into an Exchange Agreement (the “Series L Agreement”) with Alcimede LLC. Pursuant to the Series L Agreement,
the Company issued to Alcimede LLC 250,000 shares of the Series L Preferred Stock in exchange for the 250,000 shares of Series K Preferred
Stock. The shares of Series K Preferred Stock were cancelled. The Series L Preferred Stock has been convertible since December 1, 2020
(as compared to the Series K Preferred Stock which was convertible immediately) and the Series L Preferred Stock is not entitled to receive
any dividends (unlike the Series K Preferred Stock, which was entitled to share in any dividends payable on the Common Stock).
During
the year ended December 31, 2022, Mr. Diamantis loaned the Company $1.1 million, which was used by the Company to repay a portion of
the amounts past due for principal and interest under a promissory note, for which Mr. Diamantis was a guarantor. During the year ended
December 31, 2021, Mr. Diamantis loaned the Company $0.9 million, the majority of which was used for working capital purposes. During
the years ended December 31, 2022 and 2021, the Company repaid Mr. Diamantis $0.2 million and $0.9 million, respectively. On June 30,
2020, the Company exchanged the total amount owed to Mr. Diamantis on that date for outstanding loans and accrued interest, net of repayments,
which was approximately $18.8 million, for shares of the Company’s Series M Preferred Stock. The Series M Preferred Stock is more
fully discussed below.
During
the years ended December 31, 2022 and 2021, the Company incurred interest expense of $0.1 million and $0.1 million, respectively, on
the loans from Mr. Diamantis. During the year ended December 31, 2022, the Company paid $0.4 million of accrued interest owed to Mr.
Diamantis. As of December 31, 2022 and 2021, accrued interest on the loans from Mr. Diamantis totaled $0 and $0.3 million, respectively.
Interest accrues on loans from Mr. Diamantis at a rate of 10% on the majority of the amounts loaned. In addition, the Company incurs
interest expense related to the amounts Mr. Diamantis borrows from third-parties to loan to the Company.
On
June 9, 2020, the Company filed a certificate of designation to authorize 30,000 shares of its Series M Preferred Stock with a stated
value of $1,000 per share. On June 30, 2020, the Company and Mr. Diamantis entered into an exchange agreement wherein Mr. Diamantis agreed
to the extinguishment of the Company’s indebtedness to him totaling $18.8 million, including accrued interest, on that date in
exchange for 22,000 shares of the Company’s Series M Preferred Stock with a par value of $0.01 per share. As a result of the exchange,
the Company recorded a deemed dividend of approximately $3.2 million in the year ended December 31, 2020, which represented the difference
between the $18.8 million of debt and accrued interest exchanged and the value of the Series M Preferred Stock of $22.0 million.
The
terms of the Series M Preferred Stock are set forth under “Description of Capital Stock”. In particular: (i) each holder
of the Series M Preferred Stock shall be entitled to vote on all matters submitted to a vote of the holders of the Company’s common
stock. Regardless of the number of shares of Series M Preferred Stock outstanding and so long as at least one share of Series M Preferred
Stock is outstanding, the outstanding shares of Series M Preferred Stock shall have the number of votes, in the aggregate, equal to 51%
of all votes entitled to be voted at any meeting of stockholders or action by written consent. Each outstanding share of the Series M
Preferred Stock shall represent its proportionate share of the 51% allocated to the outstanding shares of Series M Preferred Stock in
the aggregate. The Series M Preferred Stock shall vote with the common stock and any other voting securities as if they were a single
class of securities; (ii) each share of the Series M Preferred Stock is convertible into shares of the Company’s common stock at
a conversion price equal to 90% of the average closing price of the Company’s common stock on the ten trading days immediately
prior to the conversion date but in any event not less than the par value of the Company’s common stock; and (iii) dividends at
the rate per annum of 10% of the stated value per share shall accrue on each outstanding share of Series M Preferred Stock
from and after the date of the original issuance of such share of Series M Preferred Stock (subject to appropriate adjustment in the
event of any stock dividend, stock split, combination or other similar recapitalization). The dividends shall accrue from day to day,
whether or not declared, and shall be cumulative and non-compounding; provided, however, that such dividend shall be payable
only when, as, and if declared by the Board of Directors and the Company shall be under no obligation to pay such dividends. No cash
dividends shall be paid on the Company’s common stock unless the dividends are paid on the Series M Preferred Stock.
On
August 13, 2020, Mr. Diamantis entered into a Voting Agreement and Irrevocable Proxy with the Company, Mr. Lagan and Alcimede LLC (of
which Mr. Lagan is the sole manager) pursuant to which Mr. Diamantis granted an irrevocable proxy to Mr. Lagan to vote the Series M Preferred
Stock held by Mr. Diamantis. Mr. Diamantis has retained all other rights under the Series M Preferred Stock.
On
August 27, 2021, the Company entered into an exchange agreement with Mr. Diamantis. Pursuant to the exchange agreement, Mr. Diamantis
exchanged 570 shares of his Series M Preferred Stock for 9,500 shares of common stock and warrants to purchase 4,750 shares of the Company’s
common stock at an exercise price of $70.00 per share. The warrants have a three-year term and, as of December 31, 2022, are exercisable
into 3.7 billion shares of the Company’s common stock at an exercise price of $0.00009 per share as a result of down-round provision
features.
On
September 27, 2019, the Company issued a promissory note to a lender in the principal amount of $1.9 million, which was guaranteed
by Mr. Diamantis. The payments due on November 8, 2019 and December 26, 2019 were not made. In February 2020, Mr. O’Killough,
the lender, sued the Company and Mr. Diamantis, as guarantor, in New York State Supreme Court for the County of New York, for
approximately $2.2 million for non-payment of the promissory note. In May 2020, the Company, Mr. Diamantis, as guarantor, and Mr.
O’Killough entered into a Stipulation providing for a payment of a total of $2.2 million (which included accrued
“penalty” interest as of that date) in installments through November 1, 2020. The Company made payments totaling
$450,000 in 2020. On January 18, 2022, Mr. Diamantis paid $750,000 and the remaining balance was due 120 days thereafter. Mr.
O’Killough agreed to forebear from any further enforcement action until then. On various dates during the remainder of 2022,
Mr. Diamantis made additional payments to Mr. O’Killough totaling $300,000 and the Company gave Mr. Diamantis $350,000 for
further payment to Mr. O’Killough. As a result of these payments, the past due balance owed to Mr. O’Killough was $1.1
million on December 31, 2022. The Company is obligated to repay Mr. Diamantis for any payments, plus interest, that he made to Mr.
O’Killough. On January 27, 2023, the parties entered into a final settlement wherein the Company and Mr. Diamantis agreed to
settle the obligation in full for $580,000.
On
November 7, 2021, the Company entered into the Exchange and Amendment Agreements (the “November 2021 Exchange Agreements”)
with certain institutional lenders. In the November 2021 Exchange Agreements, the lenders agreed to reduce their holdings of the $4.5
million of outstanding non-convertible debentures, which includes late-payment penalties, plus accrued interest of $1.5 million, by exchanging
the indebtedness and accrued interest for shares of the Company’s Series P Convertible Redeemable Preferred Stock. Mr. Diamantis
is also a party to the November 2021 Exchange Agreements as he was a guarantor of the September 27, 2019 debenture that was included
in the exchange.
In
addition to the investment in InnovaQor’s Series B-1 Preferred Stock resulting from the sale of HTS and AMSG to InnovaQor in June
2021, at December 31, 2022 and 2021, the Company had a note receivable/related party receivable resulting from working capital
advances to InnovaQor of approximately $1.5 million and $0.4 million, respectively.
As
of July 1, 2022, the Company had an outstanding receivable from InnovaQor of $803,416. InnovaQor signed a promissory note, dated July
1, 2022, in favor of the Company that provided that InnovaQor repay the Company $883,757 on December 31, 2022. That amount
represents a 10% original issue discount above the amount outstanding on July 1, 2022.
Effective
December 31, 2022, the Company and InnovaQor agreed to restructure the promissory note in favor of the Company in the amount of
$883,757 and additional monies owed in the amount of $441,018 for a new promissory note with a principal amount of $1,457,253
(inclusive of $132,478 of a 10% original issue discount) and a maturity date of June 30, 2023 except that InnovaQor will pay 25% of
any capital it receives from new capital secured prior to the maturity date. The Note, in the event of default, bears interest at
18% per annum. During the year ended December 31, 2022, the Company recognized original issue discounts totaling $0.2 million as
interest income.
During
the years ended December 31, 2022 and 2021, the Company contracted with InnovaQor to provide ongoing health information technology-related
services totaling approximately $0.2 million and $0.2 million, respectively. In addition, InnovaQor currently subleases office space
from the Company at a cost of approximately $9,700 per month for rent and utilities.
Between
January 1, 2023 and March 31, 2023, the Company advanced $0.3 million to InnovaQor to finance its working capital requirements.
PRINCIPAL
STOCKHOLDERS
The
following table summarizes certain information regarding the beneficial ownership (as such term is defined in Rule 13d-3 under the Securities
Exchange Act of 1934, as amended (the “Exchange Act”)) of our outstanding Common Stock as of March 15, 2023 by (i)
each person known by us to be the beneficial owner of more than 5% of the outstanding Common Stock, (ii) each of our directors, (iii)
each of our executive officers, and (iv) all executive officers and directors as a group. Except as indicated in the footnotes below,
the persons and entities listed below possess sole voting and investment power with respect to their shares. The address of each of our
executive officers and directors is c/o Rennova Health, Inc., 400 South Australian Avenue, Suite 800, West Palm Beach, Florida 33401.
All of the outstanding shares of Series L Convertible Preferred Stock (“Series L Preferred Stock”) are owned by Alcimede
LLC, of which Mr. Lagan, our Chief Executive Officer, is the sole manager. Mr. Diamantis owns all of the outstanding Series M Convertible
Redeemable Preferred Stock (“Series M Preferred Stock”) and has granted to Mr. Lagan an irrevocable proxy to vote the Series
M Preferred Stock. The conversion of the Series M Preferred Stock is subject to an ownership blocker of 4.99%.
Name of Beneficial Owner | |
No. of Shares of
Common Stock
Owned | | |
Percentage of Ownership (1) | |
Seamus Lagan | |
| - | (2) | |
| 54.78 | %(2) |
| |
| | | |
| | |
Gary L. Blum | |
| - | | |
| – | |
| |
| | | |
| | |
Trevor Langley | |
| - | | |
| – | |
| |
| | | |
| | |
All Directors and Executive Officers as a Group (3 persons) (3) | |
| - | (2) | |
| 54.78 | %(2) |
| |
| | | |
| | |
Sabby Healthcare Master Fund, Ltd. (4) | |
| 2,879,347,903 | | |
| 9.99 | % |
| |
| | | |
| | |
Sabby Volatility Warrant Master Fund, Ltd. (4) | |
| 2,879,347,903 | | |
| 9.99 | % |
(1) |
Based
on 29,934,322,257 shares of Common Stock issued and outstanding as of March 15, 2023, and additional shares deemed
to be outstanding as to a particular person, in accordance with applicable rules of the Securities and Exchange Commission (the “SEC”).
Beneficial ownership is determined in accordance with SEC rules to generally include shares of Common Stock subject to options or
issuable upon conversion of convertible securities or exercise of warrants, and such shares are deemed outstanding for computing
the percentage of the person holding such options, securities or warrants, but are not deemed outstanding for computing the percentage
of any other person. |
(2) |
Alcimede
LLC of which Mr. Lagan is the sole manager, owns 250,000 shares of Series L Preferred Stock. As of March 15, 2023, these
shares of Series L Preferred Stock were convertible into 2,500,000,000 shares of Common Stock. In addition, on August 13, 2020, Mr.
Diamantis granted an irrevocable proxy to Mr. Lagan to vote the Series M Preferred Stock owned by Mr. Diamantis. As a result, as
of March 15, 2023, Mr. Lagan and Alcimede LLC owned, or had the right to vote, securities holding 54.78% of the total
voting power of the Company’s voting securities. Because the conversion price of the Series L Preferred Stock is determined
based on the market price of the shares of Common Stock, the number of shares of Common Stock into which the shares are convertible,
and the votes to which the Series L Preferred Stock is entitled, will fluctuate. |
|
|
(3) |
Includes Messrs. Lagan,
Blum and Langley. Alcimede, LLC also owns 250,000 shares of Series L Preferred Stock and Mr. Lagan has an irrevocable proxy to vote
the shares of Series M Preferred Stock owned by Mr. Diamantis, as described in the above footnote. |
|
|
(4) |
Based on Amendment No.
2 to Schedule 13G filed with the SEC on January 22, 2020. The address of each of Sabby Healthcare Master Fund, Ltd. and Sabby Volatility
Warrant Master Fund, Ltd. is c/o Ogier Fiduciary Services (Cayman) Limited, 89 Nexus Way, Camana Bay, Grand Cayman KY1-9007, Cayman
Islands. This stockholder has indicated that Hal Mintz has voting and investment power over the shares held by it. This stockholder
has indicated that Sabby Management, LLC serves as its investment manager, that Hal Mintz is the manager of Sabby Management, LLC
and that each of Sabby Management, LLC and Hal Mintz disclaims beneficial ownership over these shares except to the extent of any
pecuniary interest therein. The conversion of the debentures, the Series N Preferred Stock, the Series O Preferred Stock and the
Series P Preferred Stock and the exercise of the warrants held by these entities are subject to ownership blockers of 9.99% and 4.99%,
respectively. |
DESCRIPTION
OF CAPITAL STOCK
General
The
following descriptions are summaries of the material terms of our amended and restated certificate of incorporation and amended and restated
bylaws, and are qualified by reference to our amended and restated certificate of incorporation and amended and restated bylaws. For
more detailed information, please see copies of these documents which are included as exhibits to this registration statement. We refer
in this section to our amended and restated certificate of incorporation as our certificate of incorporation, and we refer to our amended
and restated bylaws as our bylaws.
Our
authorized capital stock consists of 250,000,000,000 shares of common stock, par value $0.0001 per share, and 5,000,000 shares of preferred
stock, par value $0.01 per share. As of May 1, 2023, 29,934,322,757 shares of our common stock were outstanding and held by two
stockholders of record.
Common
Stock
The
holders of our common stock are entitled to one vote for each share held on all matters submitted to a vote of the stockholders. The
holders of our common stock do not have any cumulative voting rights. Holders of our common stock are entitled to receive ratably any
dividends declared by the board of directors out of funds legally available for that purpose, subject to any preferential dividend rights
of any outstanding preferred stock. Our common stock has no preemptive rights, conversion rights or other subscription rights or redemption
or sinking fund provisions. In the event of our liquidation, dissolution or winding up, holders of our common stock will be entitled
to share ratably in all assets remaining after payment of all debts and other liabilities and any liquidation preference of any outstanding
preferred stock.
Preferred
Stock
Our
Board of Directors may, without further action by our stockholders, fix the rights, preferences, privileges and restrictions of up to
an aggregate of 5,000,000 shares of preferred stock in one or more series and authorize their issuance. These rights, preferences and
privileges could include dividend rights, conversion rights, voting rights, terms of redemption, liquidation preferences and the number
of shares constituting any series or the designation of such series, any or all of which may be greater than the rights of our common
stock. Any issuance of our preferred stock could adversely affect the voting power of holders of our common stock and the likelihood
that such holders would receive dividend payments and payments upon liquidation. In addition, the issuance of preferred stock could have
the effect of delaying, deferring or preventing a change of control or other corporate action.
Rennova
Series H Convertible Preferred Stock
The
following is a summary of certain terms and provisions of our Series H Convertible Preferred Stock
General.
Our board of directors has designated up to 14,202 shares of the 5,000,000 authorized shares of preferred stock as Series H Preferred
Stock. As of May 1, 2023, 10 shares of Series H Preferred Stock are issued and outstanding.
Rank.
The Series H Preferred Stock ranks with respect to a liquidation, (i) on parity with the Company’s Series L Preferred Stock, the
Company’s Series M Preferred Stock, the Company’s Series N Preferred Stock and the Company’s Series O Preferred Stock,
(ii) senior to the common stock, and (iii) junior to any other securities of the Company that are explicitly senior to the Series H Preferred
Stock.
Conversion.
Each share of the Series H Preferred Stock is convertible into shares of our common stock (subject to adjustment as provided in the
related certificate of designation of preferences, rights and limitations) at any time at the option of the holder at a conversion price
equal to the stated value of the Series H Preferred Stock of $1,000 per share divided by, as of May 1, 2023, $0.000085,
subject to adjustment. Holders of Series H Preferred Stock are prohibited from converting Series H Preferred Stock into shares of our
common stock if, as a result of such conversion, the holder, together with its affiliates, would own more than 4.99% of the total number
of shares of our common stock then issued and outstanding. However, any holder may increase or decrease such percentage to any other
percentage not in excess of 9.99%, provided that any increase in such percentage shall not be effective until 61 days after such notice
to us.
Liquidation
Preference. In the event of our liquidation, dissolution or winding-up, holders of Series H Preferred Stock will be entitled to receive
an amount equal to $1,000 per share before any distribution shall be made to the holders of any junior securities, and then will be entitled
to receive the same amount that a holder of common stock would receive if the Series H Preferred Stock were fully converted into shares
of our common stock at the conversion price (disregarding for such purposes any conversion limitations) which amounts shall be paid pari
passu with all holders of common stock.
Voting
Rights. Shares of Series H Preferred Stock generally have no voting rights, except as required by law and except that the affirmative
vote of the holders of at least a majority of the then outstanding shares of Series H Preferred Stock is required to (a) alter or change
adversely the powers, preferences or rights given to the Series H Preferred Stock, (b) amend our certificate of incorporation or other
charter documents in any manner that materially adversely affects any rights of the holders, (c) increase the number of authorized shares
of Series H Preferred Stock, or (d) enter into any agreement with respect to any of the foregoing.
Dividends.
Shares of Series H Preferred Stock are not entitled to receive any dividends, unless and until specifically declared by our board
of directors. The holders of the Series H Preferred Stock will participate, on an as-if-converted-to-common stock basis, in any dividends
to the holders of common stock.
Redemption.
We are not obligated to redeem or repurchase any shares of Series H Preferred Stock. Shares of Series H Preferred Stock are not otherwise
entitled to any redemption rights or mandatory sinking fund or analogous fund provisions.
The
full text of the Series H Preferred Stock Certificate of Designation is incorporated by reference in this prospectus. This summary is
qualified in its entirety by reference to the full text of the Series H Preferred Stock Certificate of Designation.
Rennova
Series L Convertible Preferred Stock
The
following is a summary of certain terms and provisions of our Series L Convertible Preferred Stock (the “Series L Preferred Stock”).
General.
Our Board of Directors has designated 250,000 shares of the 5,000,000 authorized shares of preferred stock as the Series L Preferred
Stock. Each share of the Series L Preferred Stock has a stated value of $1.00. As of May 1, 2023, 250,000 shares
of Series L Preferred Stock are issued and outstanding.
Voting
Rights. Each holder of the Series L Preferred Stock is entitled to vote on all matters submitted to a vote of the holders of the
Company’s common stock. Until November 30, 2020, each share of Series L Preferred Stock had the same number of votes as 40,000
shares of common stock in any vote of stockholders to approve a reverse split of the common stock. As to all other matters and, from
and after December 1, 2020, each share of the Series L Preferred Stock shall be entitled to the whole number of votes equal to the number
of shares of common stock into which it is then convertible. The Series L Preferred Stock shall vote with the common stock as if they
were a single class of securities.
Dividends.
Except for stock dividends, holders of the Series L Preferred Stock shall not be entitled to receive dividends on shares of the Series
L Preferred Stock.
Rank.
The Series L Preferred Stock ranks with respect to a liquidation, (i) on parity with the common stock, the Company’s Series H Preferred
Stock, the Company’s Series M Preferred Stock, the Company’s Series N Preferred Stock and the Company’s Series O Preferred
Stock, and (ii) junior to any other class or series of preferred stock of the Company afterwards created and ranking by its terms senior
to the Series L Preferred Stock.
Conversion.
Each share of the Series L Preferred Stock is convertible into shares of the Company’s common stock from and after December 1,
2020 at the option of the holder, into that number of shares of common stock determined by dividing the stated value of such share of
Series L Preferred Stock by the conversion price. The conversion price is equal to the average closing price of the common stock on the
10 trading days immediately prior to the conversion date.
Liquidation
Preference. Upon any liquidation, dissolution or winding up of the Company, the holders of the Series L Preferred Stock shall be
entitled to receive an amount equal to the stated value of the Series L Preferred Stock and any other fees or liquidated damages then
due and owing thereon for each share of the Series L Preferred Stock before any distribution or payment shall be made on any junior securities.
Redemption.
At any time, the Company shall have the right to redeem all, or any part, of the Series L Preferred Stock then outstanding. The Series
L Preferred Stock subject to redemption shall be redeemed by the Company in cash in an amount equal to the stated value of the shares
of the Series L Preferred Stock being redeemed.
The
full text of the Series L Preferred Stock Certificate of Designation is incorporated by reference in this prospectus. This summary is
qualified in its entirety by reference to the full text of the Series L Preferred Stock Certificate of Designation.
Rennova
Series M Convertible Redeemable Preferred Stock
The
following is a summary of certain terms and provisions of the Series M Convertible Redeemable Preferred Stock (the “Series M Preferred
Stock”).
General.
Our Board of Directors has designated 30,000 shares of the 5,000,000 authorized shares of preferred stock as the Series M Preferred Stock.
Each share of the Series M Preferred Stock has a stated value of $1,000. As of May 1, 2023, 20,810 shares of Series M Preferred
Stock are issued and outstanding.
Voting
Rights. Each holder of the Series M Preferred Stock shall be entitled to vote on all matters submitted to a vote of the holders of
the Company’s common stock. Regardless of the number of shares of Series M Preferred Stock outstanding and so long as at least
one share of Series M Preferred Stock is outstanding, the outstanding shares of Series M Preferred Stock shall have the number of votes,
in the aggregate, equal to 51% of all votes entitled to be voted at any meeting of stockholders or action by written consent. Each outstanding
share of the Series M Preferred Stock shall represent its proportionate share of the 51% allocated to the outstanding shares of Series
M Preferred Stock in the aggregate. The Series M Preferred Stock shall vote with the common stock and any other voting securities as
if they were a single class of securities.
Dividends.
Dividends at the rate per annum of 10% of the stated value per share shall accrue on each outstanding share of Series M Preferred Stock
from and after the date of the original issuance of such share of Series M Preferred Stock (the “Series M Preferred Accruing Dividends”).
The Series M Preferred Accruing Dividends shall accrue from day to day, whether or not declared, and shall be cumulative and non-compounding;
provided, however, that such Series M Preferred Accruing Dividends shall be payable only when, as, and if declared by the Board of Directors.
No cash dividends shall be paid on the common stock unless the Series M Preferred Accruing Dividends are paid.
Rank.
The Series M Preferred Stock ranks with respect to dividends or a liquidation, (i) on parity with the common stock, the Company’s
Series H Preferred Stock, the Company’s Series L Preferred Stock, the Company’s Series N Preferred Stock and the Company’s
Series O Preferred Stock, and (ii) junior to any other class or series of preferred stock of the Company afterwards created and ranking
by its terms senior to the Series M Preferred Stock.
Conversion.
Each share of the Series M Preferred Stock is convertible into shares of the Company’s common stock, at any time and from time
to time, at the option of the holder, into that number of shares of common stock determined by dividing the stated value of such share
of Series M Preferred Stock, plus any accrued declared and unpaid dividends, by the conversion price. The conversion price is equal to
90% of the average closing price of the common stock on the 10 trading days immediately prior to the conversion date. Holders of the
Series M Preferred Stock are prohibited from converting Series M Preferred Stock into shares of common stock if, as a result of such
conversion, the holder, together with its affiliates, would own more than 4.99% (or, upon election of the holder, 9.99%) of the total
number of shares of common stock then issued and outstanding. However, any holder may increase or decrease such percentage to any other
percentage not in excess of 9.99%, provided that any increase in such percentage shall not be effective until 61 days after notice to
the Company.
Liquidation
Preference. Upon any liquidation, dissolution or winding up of the Company, the holders of the Series M Preferred Stock shall be
entitled to receive an amount equal to the stated value of the Series M Preferred Stock, plus any accrued declared and unpaid dividends
thereon and any other fees or liquidated damages then due and owing thereon, for each share of the Series M Preferred Stock before any
distribution or payment shall be made on any junior securities.
Redemption.
At any time, the Company shall have the right to redeem all, or any part, of the Series M Preferred Stock then outstanding. The Series
M Preferred Stock subject to redemption shall be redeemed by the Company in cash in an amount equal to the stated value of the shares
of the Series M Preferred Stock being redeemed plus all accrued declared and unpaid dividends.
Transfer.
No holder of Series M Preferred Stock shall Transfer (as defined in the Certificate of Designation) all of any portion of its shares
of Series M Preferred Stock without the written consent of the Company.
The
full text of the Series M Preferred Stock Certificate of Designation is incorporated by reference in this prospectus. This summary is
qualified in its entirety by reference to this full text of the Series M Preferred Stock Certificate of Designation.
Rennova
Series N Convertible Preferred Stock
The
following is a summary of certain terms of the Series N Convertible Redeemable Preferred Stock (the “Series N Preferred Stock”).
General.
Our Board of Directors has designated 50,000 shares of the 5,000,000 authorized shares of preferred stock as the Series N Preferred Stock.
Each share of the Series N Preferred Stock has a stated value of $1,000. As of May 1, 2023, 2,864 shares of Series N Preferred
Stock were issued and outstanding.
Voting
Rights. Except as provided below or by law, the Series N Preferred Stock shall have no voting rights. However, as long as any shares
of Series N Preferred Stock are outstanding, the Company shall not, without the affirmative vote of the holders of a majority of the
then outstanding shares of the Series N Preferred Stock, (a) alter or change adversely the powers, preferences or rights given to the
Series N Preferred Stock or alter or amend the Certificate of Designation, (b) amend its certificate of incorporation or other charter
documents in any manner that adversely affects any rights of the holders, (c) increase the number of authorized shares of the Series
N Preferred Stock, or (d) enter into any agreement with respect to any of the foregoing.
Dividends.
Dividends at the rate per annum of 10% of the stated value per share shall accrue on each outstanding share of Series N Preferred Stock
from and after the date of the original issuance of such share of Series N Preferred Stock (the “Series N Preferred Accruing Dividends”).
The Series N Preferred Accruing Dividends shall accrue from day to day, whether or not declared, and shall be cumulative and non-compounding;
provided, however, that such Series N Preferred Accruing Dividends shall be payable only when, as, and if declared by the Board of Directors.
No cash dividends shall be paid on the common stock unless the Series N Preferred Accruing Dividends are paid.
Rank.
The Series N Preferred Stock ranks with respect to dividends or a liquidation, (i) on parity with the common stock, the Company’s
Series H Preferred Stock, the Company’s Series L Preferred Stock, the Company’s Series M Preferred Stock and the Company’s
Series O Preferred Stock, and (ii) junior to any other class or series of preferred stock of the Company afterwards created and ranking
by its terms senior to the Series N Preferred Stock.
Conversion.
Each share of the Series N Preferred Stock is convertible into shares of the Company’s common stock, at any time and from time
to time, at the option of the holder, into that number of shares of common stock determined by dividing the stated value of such share
of Series N Preferred Stock, plus any accrued declared and unpaid dividends, by the conversion price. The conversion price is equal to
90% of the lowest VWAP (as defined in the Certificate of Designation) during the 10 trading days immediately prior to the conversion
date. Holders of the Series N Preferred Stock are prohibited from converting Series N Preferred Stock into shares of common stock if,
as a result of such conversion, the holder, together with its affiliates, would own more than 4.99% (or, upon election of the holder,
9.99%) of the total number of shares of common stock then issued and outstanding. However, any holder may increase or decrease such percentage
to any other percentage not in excess of 9.99%, provided that any increase in such percentage shall not be effective until 61 days after
notice to the Company.
Liquidation
Preference. Upon any liquidation, dissolution or winding up of the Company, the holders of the Series N Preferred Stock shall be
entitled to receive an amount equal to the stated value of the Series N Preferred Stock, plus any accrued declared and unpaid dividends
thereon and any other fees or liquidated damages then due and owing thereon, for each share of the Series N Preferred Stock before any
distribution or payment shall be made on any junior securities.
Redemption.
At any time, the Company shall have the right to redeem all, or any part, of the Series N Preferred Stock then outstanding. The Series
N Preferred Stock subject to redemption shall be redeemed by the Company in cash in an amount equal to the stated value of the shares
of the Series N Preferred Stock being redeemed plus all accrued declared and unpaid dividends.
The
full text of the Series N Preferred Stock Certificate of Designation is incorporated by reference in this prospectus. This summary is
qualified in its entirety by reference to the full text of the Series N Preferred Stock Certificate of Designation.
Rennova
Series O Convertible Preferred Stock
The
following is a summary of certain terms of the Series O Convertible Redeemable Preferred Stock (the “Series O Preferred Stock”).
General.
Our Board of Directors has designated 10,000 shares of the 5,000,000 authorized shares of preferred stock as the Series O Preferred Stock.
Each share of the Series O Preferred Stock has a stated value of $1,000. As of May 1, 2023, 8,645 shares of Series O Preferred
Stock were issued and outstanding.
Voting
Rights. Except as provided below or by law, the Series O Preferred Stock shall have no voting rights. However, as long as any shares
of Series O Preferred Stock are outstanding, the Company shall not, without the affirmative vote of the holders of a majority of the
then outstanding shares of the Series O Preferred Stock, (a) alter or change adversely the powers, preferences or rights given to the
Series O Preferred Stock or alter or amend the Certificate of Designation, (b) amend its certificate of incorporation or other charter
documents in any manner that adversely affects any rights of the holders, (c) increase the number of authorized shares of the Series
O Preferred Stock, or (d) enter into any agreement with respect to any of the foregoing.
Dividends.
Dividends at the rate per annum of 10% of the stated value per share shall accrue on each outstanding share of Series O Preferred Stock
from and after the date of the original issuance of such share of Series O Preferred Stock (the “Series O Preferred Accruing Dividends”).
The Series O Preferred Accruing Dividends shall accrue from day to day, whether or not declared, and shall be cumulative and non-compounding;
provided, however, that such Series O Preferred Accruing Dividends shall be payable only when, as, and if declared by the Board of Directors.
No cash dividends shall be paid on the common stock unless the Series O Preferred Accruing Dividends are paid.
Rank.
The Series O Preferred Stock ranks with respect to dividends or a liquidation, (i) on parity with the common stock, the Company’s
Series H Preferred Stock, the Company’s Series L Preferred Stock, the Company’s Series M Preferred Stock and the Company’s
Series N Preferred Stock, and (ii) junior to any other class or series of preferred stock of the Company afterwards created and ranking
by its terms senior to the Series O Preferred Stock.
Conversion.
Each share of the Series O Preferred Stock is convertible into shares of the Company’s common stock, at any time and from time
to time, at the option of the holder, into that number of shares of common stock determined by dividing the stated value of such share
of Series O Preferred Stock, plus any accrued declared and unpaid dividends, by the conversion price. The conversion price is equal to
90% of the lowest VWAP (as defined in the Certificate of Designation) during the 10 trading days immediately prior to the conversion
date. Holders of the Series O Preferred Stock are prohibited from converting Series O Preferred Stock into shares of common stock if,
as a result of such conversion, the holder, together with its affiliates, would own more than 9.99% of the total number of shares of
common stock then issued and outstanding. However, any holder may increase or decrease such percentage to any other percentage not in
excess of 9.99%, provided that any increase in such percentage shall not be effective until 61 days after notice to the Company.
Liquidation
Preference. Upon any liquidation, dissolution or winding up of the Company, the holders of the Series O Preferred Stock shall be
entitled to receive an amount equal to the stated value of the Series O Preferred Stock, plus any accrued declared and unpaid dividends
thereon and any other fees or liquidated damages then due and owing thereon, for each share of the Series O Preferred Stock before any
distribution or payment shall be made on any junior securities.
Redemption.
At any time, the Company shall have the right to redeem all, or any part, of the Series O Preferred Stock then outstanding. The Series
O Preferred Stock subject to redemption shall be redeemed by the Company in cash in an amount equal to the stated value of the shares
of the Series O Preferred Stock being redeemed plus all accrued declared and unpaid dividends.
The
full text of the Series O Preferred Stock Certificate of Designation is incorporated by reference in this prospectus. This summary is
qualified in its entirety by reference to the full text of the Series O Preferred Stock Certificate of Designation.
Rennova
Series P Convertible Preferred Stock
The
following is a summary of certain terms of the Series P Convertible Redeemable Preferred Stock (the “Series P Preferred Stock”).
General.
The Company’s Board of Directors has designated 30,000 shares of the 5,000,000 authorized shares of preferred stock as the Series
P Preferred Stock. Each share of the Series P Preferred Stock has a stated value of $1,000. As of May 1, 2023, 10,195 shares
of Series P Preferred Stock were issued and outstanding.
Voting
Rights. Except as provided below or by law, the Series P Preferred Stock shall have no voting rights. However, as long as any shares
of Series P Preferred Stock are outstanding, the Company shall not, without the affirmative vote of the holders of a majority of the
then outstanding shares of the Series P Preferred Stock, (a) alter or change adversely the powers, preferences or rights given to the
Series P Preferred Stock or alter or amend the Certificate of Designation, (b) amend its certificate of incorporation or other charter
documents in any manner that adversely affects any rights of the holders, (c) increase the number of authorized shares of the Series
P Preferred Stock, or (d) enter into any agreement with respect to any of the foregoing.
Dividends.
Dividends at the rate per annum of 10% of the stated value per share shall accrue on each outstanding share of Series P Preferred Stock
from and after the date of the original issuance of such share of Series P Preferred Stock (the “Series P Preferred Accruing Dividends”).
The Series P Preferred Accruing Dividends shall accrue from day to day, whether or not declared, and shall be cumulative and non-compounding;
provided, however, that such Series P Preferred Accruing Dividends shall be payable only when, as, and if declared by the
Board of Directors. No cash dividends shall be paid on the common stock unless the Series P Preferred Accruing Dividends are paid.
Rank.
The Series P Preferred Stock ranks with respect to dividends or a liquidation, (i) on parity with the common stock, the Company’s
Series H Preferred Stock, the Company’s Series L Preferred Stock, the Company’s Series M Preferred Stock, the Company’s
Series N Preferred Stock, and the Company’s Series O Preferred Stock, and (ii) junior to any other class or series of preferred
stock of the Company afterwards created and ranking by its terms senior to the Series P Preferred Stock.
Conversion.
Each share of the Series P Preferred Stock is convertible into shares of the Company’s common stock, at any time and from time
to time, at the option of the holder, into that number of shares of common stock determined by dividing the stated value of such share
of Series P Preferred Stock, plus any accrued declared and unpaid dividends, by the conversion price. The conversion price is equal to
90% of the lowest VWAP during the 10 trading days immediately prior to the conversion date. Holders of the Series P Preferred Stock are
prohibited from converting Series P Preferred Stock into shares of common stock if, as a result of such conversion, the holder, together
with its affiliates, would own more than 9.99% of the total number of shares of common stock then issued and outstanding. However, any
holder may increase or decrease such percentage to any other percentage not in excess of 9.99%, provided that any increase in such percentage
shall not be effective until 61 days after notice to the Company.
Liquidation
Preference. Upon any liquidation, dissolution or winding up of the Company, the holders of the Series P Preferred Stock shall be
entitled to receive an amount equal to the stated value of the Series P Preferred Stock, plus any accrued declared and unpaid dividends
thereon and any other fees or liquidated damages then due and owing thereon, for each share of the Series P Preferred Stock before any
distribution or payment shall be made on any junior securities.
Redemption.
At any time the Company shall have the right to redeem all, or any part, of the Series P Preferred Stock then outstanding. The Series
P Preferred Stock subject to redemption shall be redeemed by the Company in cash in an amount equal to the stated value of the shares
of the Series P Preferred Stock being redeemed plus all accrued declared and unpaid dividends.
The
full text of the Series P Preferred Stock Certificate of Designation is incorporated by reference in this prospectus. This summary is
qualified in its entirety by reference to the full text of the Series P Certificate of Designation.
Warrants
As
of December 31, 2022, we had outstanding warrants to purchase 511,333,351,090 shares of common stock at a weighted average exercise
price of $0.00009 per share which expire at various dates through September 2024.
The
Series B Warrants were issued to the Selling Stockholders and other existing institutional investors in private placements of convertible
debentures and warrants on March 21, 2017. The Series B Warrants are exercisable through March 31, 2024. As of March 31, 2023,
the Series B Warrants are exercisable into an aggregate of 127,702,257,133 shares of common stock at an exercise price of $0.00009.
The exercise price of the Series B Warrants, and the number of shares of common stock into which they are exercisable, are subject
to reset in the event of offerings or other issuances of common stock, or rights to purchase common stock, at a price below the then
exercise price, as well as other customary anti-dilution protections. Since the original issuance of the Series B Warrants, the number
of shares of common stock into which they are exercisable has significantly increased and the exercise price has significantly decreased
as a result of equity issuances by the Company, and they are subject to further adjustment depending on the terms and prices of equity
issuances (or deemed issuances) in the future.
The holders of the Series B Warrants are prohibited
from exercising the Series B Warrants for common stock if, as a result of such exercise, the holder, together with its affiliates, would
own more than 4.99% of the total number of shares of common stock then outstanding; provided that such percentage may be increased or
decreased to any other percentage not in excess of 9.99% by notice to the Company. The Selling Stockholders have increased the percentage
limitation to which their Series B Warrants are subject to 9.99%.
Anti-Takeover
Effects of Delaware Law and Our Certificate of Incorporation and Bylaws
Certain
provisions of Delaware law, our certificate of incorporation and our bylaws contain provisions that could have the effect of delaying,
deferring or discouraging another party from acquiring control of us. These provisions, which are summarized below, may have the effect
of discouraging coercive takeover practices and inadequate takeover bids. These provisions are also designed, in part, to encourage persons
seeking to acquire control of us to first negotiate with our board of directors. We believe that the benefits of increased protection
of our potential ability to negotiate with an unfriendly or unsolicited acquirer outweigh the disadvantages of discouraging a proposal
to acquire us because negotiation of these proposals could result in an improvement of their terms.
Board
Composition and Filling Vacancies
Our
bylaws provide that any Director or the entire Board may be removed at any time, with or without cause, by the holders of a majority
of the shares then entitled to vote at an election of directors. Directors shall be elected at the annual meeting of the stockholders
and each Director elected shall hold office until his successor is elected and qualified; provided, however, that unless otherwise restricted
by the Certificate of Incorporation or by law, any Director or the entire Board may be removed, either with or without cause, from the
Board at any meeting of stockholders by a majority of the stock represented and entitled to vote thereat. Vacancies on the Board by reason
of death, resignation, retirement, disqualification, removal from office, or otherwise, and newly created directorships resulting from
any increase in the authorized number of directors may be filled by a majority of the directors then in office, although less than a
quorum, or by a sole remaining Director. The Directors so chosen shall hold office until the next annual election of Directors and until
their successors are duly elected and shall qualify, unless sooner displaced.
Meetings
of Stockholders
Our
certificate of incorporation and bylaws provide that only a majority of the members of our board of directors then in office may call
special meetings of stockholders and only those matters set forth in the notice of the special meeting may be considered or acted upon
at a special meeting of stockholders. Our bylaws limit the business that may be conducted at an annual meeting of stockholders to those
matters properly brought before the meeting.
Advance
Notice Requirements
Our
bylaws establish advance notice procedures with regard to stockholder proposals relating to the nomination of candidates for election
as directors or new business to be brought before meetings of our stockholders. These procedures provide that notice of stockholder proposals
must be timely given in writing to our corporate secretary prior to the meeting at which the action is to be taken. Generally, to be
timely, notice must be received at our principal executive offices not less than 90 days nor more than 120 days prior to the first anniversary
date of the annual meeting for the preceding year. Our bylaws specify the requirements as to form and content of all stockholders’
notices. These requirements may preclude stockholders from bringing matters before the stockholders at an annual or special meeting.
Amendment
to Bylaws
The
Board may from time to time make, amend, supplement or repeal the Company’s Bylaws by vote of a majority of the Board, and the
stockholders may change or amend or repeal these Bylaws by the affirmative vote of the majority of holders of the common stock. In addition
to and not in limitation of the foregoing, the Company’s Bylaws or any of them may be amended or supplemented in any respect at
any time, either: (i) at any meeting of stockholders, provided that any amendment or supplement proposed to be acted upon at any such
meeting shall have been described or referred to in the notice of such meeting; or (ii) at any meeting of the Board, provided that any
amendment or supplement proposed to be acted upon at any such meeting shall have been described or referred to in the notice of such
meeting or an announcement with respect thereto shall have been made at the last previous Board meeting, and provided further that no
amendment or supplement adopted by the Board shall vary or conflict with any amendment or supplement adopted by the stockholders.
Section
203 of the Delaware General Corporation Law
We
are subject to the provisions of Section 203 of the Delaware General Corporation Law. In general, Section 203 prohibits a publicly held
Delaware corporation from engaging in a “business combination” with an “interested stockholder” for a three-year
period following the time that this stockholder becomes an interested stockholder, unless the business combination is approved in a prescribed
manner. Under Section 203, a business combination between a corporation and an interested stockholder is prohibited unless it satisfies
one of the following conditions:
|
● |
before
the stockholder became interested, our board of directors approved either the business combination or the transaction which resulted
in the stockholder becoming an interested stockholder; |
|
● |
upon
consummation of the transaction which resulted in the stockholder becoming an interested stockholder, the interested stockholder
owned at least 85% of the voting stock of the corporation outstanding at the time the transaction commenced, excluding for purposes
of determining the voting stock outstanding, shares owned by persons who are directors and also officers, and employee stock plans,
in some instances, but not the outstanding voting stock owned by the interested stockholder; or |
|
● |
at
or after the time the stockholder became interested, the business combination was approved by our board of directors and authorized
at an annual or special meeting of the stockholders by the affirmative vote of at least two-thirds of the outstanding voting stock
which is not owned by the interested stockholder. |
Section
203 defines a business combination to include:
|
● |
any
merger or consolidation involving the corporation and the interested stockholder; |
|
● |
any
sale, transfer, lease, pledge or other disposition involving the interested stockholder of 10% or more of the assets of the corporation; |
|
● |
subject
to exceptions, any transaction that results in the issuance or transfer by the corporation of any stock of the corporation to the
interested stockholder; |
|
● |
subject
to exceptions, any transaction involving the corporation that has the effect of increasing the proportionate share of the stock of
any class or series of the corporation beneficially owned by the interested stockholder; and |
|
● |
the
receipt by the interested stockholder of the benefit of any loans, advances, guarantees, pledges or other financial benefits provided
by or through the corporation. |
In
general, Section 203 defines an interested stockholder as any entity or person beneficially owning 15% or more of the outstanding voting
stock of the corporation and any entity or person affiliated with or controlling or controlled by the entity or person.
Trading
Market
Our
common stock is traded on the OTC Pink under the trading symbol “RNVA.”
Transfer
Agent and Registrar
The
transfer agent and registrar for our common stock is Computershare Trust Company, N.A. The transfer agent and registrar’s address
is 250 Royall Street, Canton, Massachusetts 02021.
DESCRIPTION
OF THE SECURITIES WE ARE OFFERING
Common
Stock
The
material terms and provisions of our common stock are described under the caption “Description of Capital Stock” starting
on page 46 of this prospectus.
SHARES
ELIGIBLE FOR FUTURE SALE
Future
sales of substantial amounts of our common stock in the public market, including shares issued upon exercise of outstanding warrants,
or the conversion of outstanding preferred stock or other convertible securities, or the anticipation of these sales, could adversely
affect prevailing market prices from time to time and could impair our ability to raise equity capital in the future.
Rule
144
In
general, under Rule 144, any person who is not our affiliate and has held their shares for at least six months, including the holding
period of any prior owner other than one of our affiliates, may sell shares without restriction, subject to the availability of current
public information about us. In addition, under Rule 144, any person who is not an affiliate of ours and has held their shares for at
least one year, including the holding period of any prior owner other than one of our affiliates, would be entitled to sell an unlimited
number of shares without regard to whether current public information about us is available. A person who is our affiliate or who was
our affiliate at any time during the preceding three months, and who has beneficially owned restricted securities for at least six months,
including the holding period of any prior owner other than one of our affiliates, is entitled to sell a number of shares within any three-month
period that does not exceed the greater of:
|
● |
1%
of the number of shares of our common stock then outstanding, which currently would equal approximately 299,343,200 shares;
or |
|
● |
the
average weekly trading volume of our common stock on the OTC Pink market during the four calendar weeks preceding the filing of a
notice on Form 144 with respect to the sale. |
Sales
under Rule 144 by our affiliates are also subject to manner of sale provisions and notice requirements, and to the availability of current
public information about us.
SELLING
STOCKHOLDERS
The
shares of common stock being offered by the Selling Stockholders are those issuable to the Selling Stockholders upon exercise of Series
B Warrants. We are registering the shares of common stock in order to permit the Selling Stockholders to offer the shares for resale
from time to time. Except for the ownership of the Series B Warrants, as well as shares of common stock, preferred stock, convertible
debentures, debentures and warrants, the Selling Stockholders have not had any material relationship with us within the past three years.
The
table below lists the Selling Stockholders and other information regarding the beneficial ownership of the shares of common stock by
each of the Selling Stockholders. The first column lists the number of shares of common stock beneficially owned by each Selling
Stockholder, as of December 1, 2022, assuming exercise of the Series B Warrants and other warrants, as well as conversion of
convertible debentures and convertible preferred stock held by the Selling Stockholders on that date, subject to any limitations on
exercises or conversions.
In
addition, under the terms of the Series B Warrants and certain other securities, a Selling Stockholder may not exercise the Series B
Warrants or convert or exercise such other securities to the extent such exercise or conversion would cause such Selling Stockholder,
together with its affiliates and attribution parties, to beneficially own a number of shares of Common Stock which would exceed 9.99%
of our then outstanding Common Stock following such exercise or conversion, excluding for purposes of such determination shares of Common
Stock issuable upon exercise of the Series B Warrants or conversion or exercise of such other securities which have not been exercised
or converted. The Selling Stockholders may sell all, some or none of their shares in this offering. See “Plan of Distribution.”
Name of Selling Stockholder | |
Number of shares of Common Stock Owned Prior to Offering (2) | | |
% of shares of Common Stock Owned Prior to Offering | | |
Maximum Number of Shares of Common Stock to be Sold Pursuant to this Prospectus (2) | | |
Number of shares of Common Stock Owned After Offering | | |
% of shares of Common Stock Owned After Offering | |
| |
| | |
| | |
| | |
| | |
| |
Sabby Healthcare Master Fund, Ltd. (1) | |
| 580,119,436,115 | (3) | |
| 9.99 | %(5) | |
| 8,494,356,530 | | |
| 571,625,079,585 | | |
| 9.99 | %(5) |
Sabby Volatility Warrant Master Fund, Ltd. (1) | |
| 200,427,905,641 | (4) | |
| 9.99 | %(5) | |
| 1,483,743,470 | | |
| 198,944,162,171 | | |
| 9.99 | %(5) |
(1) |
This
stockholder has indicated that Hal Mintz has voting and investment power over the shares held by it. This stockholder has indicated
that Sabby Management, LLC serves as its investment manager, that Hal Mintz is the manager of Sabby Management, LLC and that each
of Sabby Management, LLC and Hal Mintz disclaims beneficial ownership over these shares except to the extent of any pecuniary interest
therein. |
(2) |
The
actual number of shares of Common Stock offered hereby and included in the registration statement of which this prospectus is a part
includes, in accordance with Rule 416 under the Securities Act, such indeterminate number of additional shares of our Common Stock
as may become issuable in connection with any proportionate adjustment for any stock splits, stock combinations, stock dividends,
recapitalizations, anti-dilution adjustments or similar events with respect to our Common Stock. |
(3) |
Includes
967,085,094 shares of Common Stock and the following shares of Common Stock underlying convertible securities that are convertible
or exercisable within 60 days of December 1, 2022: (i) 14,388,916,667 shares of Common Stock issuable upon conversion
of Debentures; (ii) 108,708,949,909 shares of Common Stock issuable upon exercise of Series B Warrants; (iii) 315,197,740,000
shares of Common Stock issuable upon exercise of other warrants; (iv) 32,225,688,889 shares of Common Stock issuable upon
conversion of Series N Preferred Stock; (v) 55,000,000,000 shares of Common Stock issuable upon conversion of Series O Preferred
Stock; and (vi) 53,631,055,556 shares of Common Stock issuable upon conversion of Series P Preferred Stock. The conversion
and exercise prices of the foregoing securities are subject to adjustment. The conversion of the Debentures and Preferred Stock and
the exercise of the Warrants held by this entity are subject to ownership blockers of 9.99%. |
(4) |
Includes
1,160,494,462 shares of Common Stock and the following shares of Common Stock underlying convertible securities that are convertible
or exercisable within 60 days of December 1, 2022: (i) 14,388,916,667 shares of Common Stock issuable upon conversion
of Debentures; (ii) 18,993,307,224 shares of Common Stock issuable upon exercise of Series B Warrants; (iii) 64,738,909,510
shares of Common Stock issuable upon exercise of other warrants; (iv) 41,501,000,000 shares of Common Stock issuable upon
conversion of Series O Preferred Stock; and (v) 59,645,277,778 shares of Common Stock issuable upon conversion of Series P Preferred
Stock. The conversion and exercise prices of the foregoing securities are subject to adjustment. The conversion of the Debentures
and Preferred Stock and the exercise of the Warrants held by this entity are subject to ownership blockers of 9.99%. |
(5) |
Represents
the aggregate combined percentage of shares beneficially owned by Sabby Healthcare Master Fund, Ltd. and Sabby Volatility Warrant
Master Fund, Ltd. The conversion of debentures and preferred stock and the exercise of Warrants held by these entities
are subject to ownership blockers of 9.99%. |
PLAN
OF DISTRIBUTION
Each
Selling Stockholder of the securities and any of their pledgees, assignees and successors-in-interest may, from time to time, sell any
or all of their securities covered hereby on the principal trading market or any other stock exchange, market or trading facility on
which the securities are traded or in private transactions. These sales shall be at the fixed price of $0.00014 until such time
as our common stock is quoted on the OTCQB or OTCQX marketplace, or listed on a national securities exchange. Thereafter, these sales
may be made at negotiated prices or at varying prices determined at the time of sale. A Selling Stockholder may use any one or more of
the following methods when selling securities:
|
● |
ordinary
brokerage transactions and transactions in which the broker-dealer solicits purchasers; |
|
● |
block
trades in which the broker-dealer will attempt to sell the securities as agent but may position and resell a portion of the block
as principal to facilitate the transaction; |
|
● |
purchases
by a broker-dealer as principal and resale by the broker-dealer for its account; |
|
● |
an
exchange distribution in accordance with the rules of the applicable exchange; |
|
● |
privately
negotiated transactions; |
|
● |
settlement
of short sales; |
|
● |
in
transactions through broker-dealers that agree with the Selling Stockholders to sell a specified number of such securities at a stipulated
price per security; |
|
● |
through
the writing or settlement of options or other hedging transactions, whether through an options exchange or otherwise; |
|
● |
a
combination of any such methods of sale; or |
|
● |
any
other method permitted pursuant to applicable law. |
The
Selling Stockholders may also sell securities under Rule 144 or any other exemption from registration under the Securities Act, if available,
rather than under this prospectus.
Broker-dealers
engaged by the Selling Stockholders may arrange for other broker-dealers to participate in sales. Broker-dealers may receive commissions
or discounts from the Selling Stockholders (or, if any broker dealer acts as agent for the purchaser of securities, from the purchaser)
in amounts to be negotiated, but, except as set forth in a supplement to this prospectus, in the case of an agency transaction not in
excess of a customary brokerage commission in compliance with FINRA Rule 2440; and in the case of a principal transaction a markup or
markdown in compliance with FINRA IM-2440.
In
connection with the sale of the securities or interests therein, the Selling Stockholders may enter into hedging transactions with broker-dealers
or other financial institutions, which may in turn engage in short sales of the securities in the course of hedging the positions they
assume. The Selling Stockholders may also sell securities short and deliver these securities to close out their short positions, or loan
or pledge the securities to broker-dealers that in turn may sell these securities. The Selling Stockholders may also enter into option
or other transactions with broker-dealers or other financial institutions or create one or more derivative securities which require the
delivery to such broker-dealer or other financial institution of securities offered by this prospectus, which securities such broker-dealer
or other financial institution may resell pursuant to this prospectus (as supplemented or amended to reflect such transaction).
The
Selling Stockholders and any broker-dealers or agents that are involved in selling the securities may be deemed to be “underwriters”
within the meaning of the Securities Act in connection with such sales. In such event, any commissions received by such broker-dealers
or agents and any profit on the resale of the securities purchased by them may be deemed to be underwriting commissions or discounts
under the Securities Act. Each Selling Stockholder has informed the Company that it does not have any written or oral agreement or understanding,
directly or indirectly, with any person to distribute the securities.
The
Company is required to pay certain fees and expenses incurred by the Company incident to the registration of the securities. The Company
has agreed to indemnify the Selling Stockholders against certain losses, claims, damages and liabilities, including liabilities under
the Securities Act.
The
resale securities will be sold only through registered or licensed brokers or dealers if required under applicable state securities laws.
In addition, in certain states, the resale securities covered hereby may not be sold unless they have been registered or qualified for
sale in the applicable state or an exemption from the registration or qualification requirement is available and is complied with.
Under
applicable rules and regulations under the Exchange Act, any person engaged in the distribution of the resale securities may not simultaneously
engage in market making activities with respect to the common stock for the applicable restricted period, as defined in Regulation M,
prior to the commencement of the distribution. In addition, the Selling Stockholders will be subject to applicable provisions of the
Exchange Act and the rules and regulations thereunder, including Regulation M, which may limit the timing of purchases and sales of the
common stock by the Selling Stockholders or any other person. We will make copies of this prospectus available to the Selling Stockholders
and have informed them of the need to deliver a copy of this prospectus to each purchaser at or prior to the time of the sale (including
by compliance with Rule 172 under the Securities Act).
LEGAL
MATTERS
The
validity of the securities offered by this prospectus will be passed upon for us by Shutts & Bowen LLP, Miami, Florida.
EXPERTS
The
consolidated balance sheets of Rennova and subsidiaries as of December 31, 2022 and 2021, and the related consolidated
statements of operations, stockholders’ deficit, and cash flows for each of the years in the two-year period ended December 31,
2022, have been audited by Haynie & Company, independent registered public accounting firm, as stated in their report which
is incorporated by reference herein. Such financial statements have been incorporated by reference herein in reliance on the report of
such firm given upon its authority as experts in accounting and auditing.
WHERE
YOU CAN FIND ADDITIONAL INFORMATION
We
have filed with the SEC a registration statement on Form S-1 under the Securities Act with respect to the securities being offered by
this prospectus. This prospectus does not contain all of the information in the registration statement and its exhibits. For further
information with respect to us and the securities offered by this prospectus, we refer you to the registration statement and its exhibits.
Statements contained in this prospectus as to the contents of any contract or any other document referred to are not necessarily complete,
and in each instance, we refer you to the copy of the contract or other document filed as an exhibit to the registration statement. Each
of these statements is qualified in all respects by this reference.
You
can read our SEC filings, including the registration statement, over the Internet at the SEC’s website at www.sec.gov. You may
also read and copy any document we file with the SEC at its public reference facilities at 100 F Street N.E., Washington, D.C. 20549.
You may also obtain copies of these documents at prescribed rates by writing to the Public Reference Section of the SEC at 100 F Street
N.E., Washington, D.C. 20549. Please call the SEC at 1-800-SEC-0330 for further information on the operation of the public reference
facilities.
We
are subject to the information and periodic reporting requirements of the Exchange Act, and we file periodic reports, proxy statements
and other information with the SEC. These periodic reports, proxy statements and other information are available for inspection and copying
at the public reference room and website of the SEC referred to above. We maintain a website at http://www.rennovahealth.com. You may
access our annual reports on Form 10-K, quarterly reports on Form 10-Q, current reports on Form 8-K and amendments to those reports filed
or furnished pursuant to Section 13(a) or 15(d) of the Exchange Act with the SEC free of charge at our website as soon as reasonably
practicable after such material is electronically filed with, or furnished to, the SEC. The information contained in, or that can be
accessed through, our website is not incorporated by reference in, and is not part of, this prospectus.
INCORPORATION
OF CERTAIN INFORMATION BY REFERENCE
The
following documents filed by Rennova Health, Inc. with the SEC are incorporated by reference into this prospectus. You should carefully
read and consider all of these documents before making an investment decision:
|
● |
Annual
Report on Form
10-K for the year ended December 31, 2022, filed with the SEC on April 17, 2023; and |
|
● |
Description
of the common stock contained in the Company’s Registration Statement on Form S-4 (File No. 333-205733) deemed effective by
the SEC on September 22, 2015. |
All
documents that we file with the SEC under Sections 13(a), 13(c), 14 or 15(d) of the Exchange Act, after the initial registration
statement and prior to the effectiveness of the registration statement as well as on or after the date of this prospectus and
prior to the termination of this offering are also incorporated herein by reference and will automatically update and, to the extent
described above, supersede information contained or incorporated by reference in this prospectus and previously filed documents that
are incorporated by reference in this prospectus. However, anything herein to the contrary notwithstanding, no document, exhibit or
information or portion thereof that we have “furnished” or may in the future “furnish” to (rather than
“file” with) the SEC, including, without limitation, any document, exhibit or information filed pursuant to Item 2.02,
Item 7.01 and certain exhibits furnished pursuant to Item 9.01 of our Current Reports on Form 8-K, shall be incorporated by
reference into this prospectus.
We
will provide to each person, including any beneficial owner, to whom a prospectus is delivered, a copy of any or all of the reports or
documents that have been incorporated by reference into this prospectus but not delivered with this prospectus. We will provide these
reports upon written or oral request at no cost to the requester. Please direct your request, either in writing or by telephone, to the
Corporate Secretary, Rennova Health, Inc., 400 South Australian Avenue, Suite 800, West Palm Beach, Florida 33401, telephone number (561)
855-1626. We maintain a website at http://www.rennovahealth.com. You may access our annual reports on Form 10-K, quarterly reports on
Form 10-Q, current reports on Form 8-K and amendments to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Exchange
Act with the SEC free of charge at our website as soon as reasonably practicable after such material is electronically filed with, or
furnished to, the SEC. The information contained in, or that can be accessed through, our website is not incorporated by reference in,
and is not part of, this prospectus.
9,978,100,000
Shares of Common Stock
PROSPECTUS
May
12, 2023
Rennova Health (CE) (USOTC:RNVA)
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