Securities and Exchange Commission v. Mimedx Group, Inc.

CourtDistrict Court, S.D. New York
DecidedMarch 28, 2022
Docket1:19-cv-10927
StatusUnknown

This text of Securities and Exchange Commission v. Mimedx Group, Inc. (Securities and Exchange Commission v. Mimedx Group, Inc.) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Securities and Exchange Commission v. Mimedx Group, Inc., (S.D.N.Y. 2022).

Opinion

UNITED STATES DISTRICT COURT

SOUTHERN DISTRICT OF NEW YORK

------------------------------X

SECURITIES AND EXCHANGE

COMMISSION,

MEMORANDUM AND ORDER Plaintiff, 19 Civ. 10927 (NRB) - against –

MIMEDX GROUP, INC., PARKER H. PETIT, WILLIAM C. TAYLOR, and MICHAEL J. SENKEN,

Defendants.

------------------------------X NAOMI REICE BUCHWALD UNITED STATES DISTRICT JUDGE

The Securities and Exchange Commission (“SEC”) has brought this action against MiMedx Group, Inc. (“MiMedx”), Parker H. Petit (“Petit”), William C. Taylor (“Taylor”), and Michael J. Senken (“Senken”). The SEC’s complaint (the “Complaint”), filed on November 26, 2019, asserts the following claims: securities fraud claims against all defendants under Section 17(a) of the Securities Act of 1933 (“Securities Act”), Section 10(b) of the Securities Exchange Act of 1934 (“Exchange Act”), and Rule 10b-5 promulgated thereunder; books and records claims against all individual defendants for violations of Exchange Act Section 13(b)(5) and of Rules 13b2-1 and 13b2-2; books and records claims against MiMedx for violations of Section 13(b)(2) of the Exchange Act; false certifications claims against Petit and Senken for violations of Rule 13a-14 of the Exchange Act; false SEC filings claims against MiMedx for violations of Section 13(a) of the Exchange Act and Rules 12b-20, 13a-1, 13a-11, and 13a-13; aiding and abetting claims against all individual defendants for violation of Exchange Act Sections 10(b), 13(a), 13(b)(2), 17(a) and Rules 12b-20, 13a-1, 13a-11, and 13a-13; control person liability against Petit and Taylor under Section 20(a) of the Exchange Act; and violation of

Section 304(a) of the Sarbanes-Oxley Act of 2002 by Petit and Senken. Before the Court is Senken’s motion to dismiss the Complaint for failure to state a claim pursuant to Federal Rule of Civil Procedure 12(b)(6). Oral argument was held on March 23, 2022. BACKGROUND I. Factual Background While the allegations in the Complaint concern activity related to Petit, Taylor, Senken, and MiMedx, we focus on those facts that are primarily relevant to the instant motion.1 a. The Defendants

MiMedx is a “regenerative medicine biotechnology company”

1 Petit and Taylor were charged in a parallel criminal action, No. 19 Crim. 850, and were both convicted on November 19, 2020. See ECF No. 68. Petit was found guilty of securities fraud and Taylor was found guilty of conspiracy to commit securities fraud. Id. Petit and Taylor were each sentenced to a one- year term of imprisonment and were fined $1,000,000 and $250,000 respectively. See 19 Crim. 850, ECF Nos. 153, 154. Petit and Taylor have appealed their sentences. See 19 Crim. 850, ECF Nos. 155, 156.

-2- headquartered in Marietta, Georgia that “sells a variety of products derived from human placental, amniotic, and umbilical tissues.” See Compl. ¶¶ 13, 17. These products include “wound care and surgical allografts (tissue grafts transplanted between unrelated individuals) . . . and an injectable amniotic liquid product.” Id. ¶ 18. MiMedx’s securities traded on the Nasdaq Global Market until 2018, including during the relevant period

from 2013 until the third quarter of 2017. Id. ¶ 13. Currently, they are traded on OTC Link. Id. On July 3, 2013, MiMedx raised $34 million in an offering, filing a Form S-3 to register an offering of new shares of stock. Id. Petit was MiMedx’s chairman and CEO from February 2009 to June 2018, with “control over the management, general operations, sales personnel, and related policies of MiMedx.” Id. ¶ 14. Taylor was MiMedx’s president and COO from 2011 to June 2018, served on the board of directors, and exercised control over the management, general operations, sales personnel, and related policies of MiMedx. Id. ¶ 15. Senken served as MiMedx’s CFO from

2011 to June 2018 and, along with Petit, signed and certified each of MiMedx’s Forms 10-K and 10-Q filed between 2013 and November 2017. Id. ¶ 16. Senken also signed management letters provided to MiMedx’s auditors from 2013 through the second quarter of 2017

-3- (to Auditor A) and for the third quarterly review of 2017 (to Auditor B). Id. Senken had previously passed the certified public accountant examination and worked as CFO of multiple companies. Id. MiMedx followed two different sales models with its customers. For its “direct sales” customers, MiMedx would recognize revenue at the time that product was shipped to the

customer. Id. ¶ 19. For other customers, MiMedx would consign products, which entailed shipping product to the customer with no expectation of payment until the product was used or implanted. Id. Revenue for this latter category of customer was recognized at the time product was used or implanted. Id. This revenue recognition approach is required by U.S. Generally Accepted Accounting Principles (“GAAP”). Pursuant to GAAP, companies cannot recognize revenue until the revenue was “realized or realizable and earned, which occurs only when each of the following conditions is met (i) persuasive evidence of an arrangement exists; (ii) delivery has occurred or services have been rendered; (iii)

the seller’s price to the buyer is fixed or determinable; and (iv) collectability is reasonably assured.” Id. ¶ 21. MiMedx disclosed its revenue recognition policy in its annual and quarterly financial filings during the relevant period. Id. ¶ 22.

-4- b. Distributor E Side Agreement From approximately 2012-2017, Distributor E sold MiMedx products to the U.S. Department of Veterans Affairs and the U.S. Department of Defense (collectively, the “VA”). Id. ¶ 134. Distributor E represented 56% of MiMedx’s total reported revenue in 2013, 34% of total reported revenue in 2014, 24% of total reported revenue in 2015, and “a declining percentage thereafter.”

Id. ¶ 135. MiMedx’s relationship with Distributor E commenced in April 2012, when the two companies entered into a written distribution agreement. Id. ¶ 137. Under the terms of the agreement, MiMedx made “direct sales” to Distributor E, and payment was due within a specific period of time after invoice. Revenue was recognized based on when the product had been shipped to Distributor E. Id. ¶¶ 137, 138. However, “[b]y at least January 1, 2013,” contrary to the terms of MiMedx and Distributor E’s written agreement, Petit and Taylor entered into a side arrangement with Distributor E that changed the sales model into a “consignment model” whereby Distributor E would not pay for product until it

received payment from the VA. Id. ¶ 139. Taylor further memorialized the terms of the side agreement in an email to Distributor E on March 8, 2013, which he did not disclose to MiMedx accounting staff, attorneys, or auditors, writing that despite the

-5- distribution agreement “stat[ing] our legal terms and obligations . . . we need flexibility that meets both our business needs,” and therefore payment would operate, as it had for the first six months of 2013, “slightly different than the way the contract is written.” Id. ¶ 170. Petit and Taylor also agreed to “credit” Distributor E for any product that was dropped, damaged, or lost, and allowed Distributor E to return product that the VA did not want to use.

Id. ¶ 145-46. Thus, under the side agreement to be consistent with GAAP, MiMedx should have recognized revenue at the time of Distributor E’s payment, rather than at the time of shipment. Id. ¶ 139. In order to implement the side agreement, Distributor E would send a daily report to MiMedx that listed products for which it had received a purchase order from the VA, including the price charged and the patient for whom the product was used. Id. ¶ 151.

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