United States v. Cockerell Dermatopathology PA

CourtDistrict Court, N.D. Texas
DecidedOctober 20, 2021
Docket3:21-cv-00672
StatusUnknown

This text of United States v. Cockerell Dermatopathology PA (United States v. Cockerell Dermatopathology PA) is published on Counsel Stack Legal Research, covering District Court, N.D. Texas primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States v. Cockerell Dermatopathology PA, (N.D. Tex. 2021).

Opinion

UNITED STATES DISTRICT COURT NORTHERN DISTRICT OF TEXAS DALLAS DIVISION UNITED STATES OF AMERICA, § § Plaintiff, § § v. § CIVIL ACTION NO. 3:21-CV-0672-B § COCKERELL § DERMATOPATHOLOGY, P.A. and § CLAY J. COCKERELL, M.D., § § Defendants. § MEMORANDUM OPINION & ORDER Before the Court is Defendants Cockerell Dermatopathology, P.A. (“CDP”) and Clay J. Cockerell, M.D. (“Cockerell”)’s Motion to Dismiss (Doc. 6) the third cause of action in the Government’s Complaint (Doc. 1) for failure to state a claim per Federal Rule of Civil Procedure 9(b). At issue here is whether the United States (“Government”) sufficiently pleaded an obligation with the particularity as required by Rule 9(b), and whether the reverse false claim is redundant of the other false claims. For the following reasons, the Court DENIES Defendants’ Motion.

- 1 - I. BACKGROUND A. Factual Background1 This is a qui tam2 suit with claims pursuant to the False Claims Act (“FCA”) for Defendants’ submission of false claims, conspiracy to violate the FCA, and failure to reimburse the federal

government for overpayments, along with federal common law claims of unjust enrichment and payment by mistake. Only the third cause of action—failure to reimburse the federal government—is at issue in this Motion to Dismiss. Scott Schuster (“Schuster”) and Dustin Rall (“Rall”) owned and served as members of the Board of Directors for the Medicine Store Pharmacy, Inc. d/b/a Rxpress Pharmacy (“Rxpress”) in Fort Worth, Texas. Doc. 1, Compl. ¶ 76. Quintan Cockerell (“Quintan”)—Cockerell’s nephew—and Luke Zeutzius (“Zeutzius”) worked as marketers for Rxpress. Id. Rxpress relied on “a

network of marketers to generate referrals for expensive ‘compound’ medications, such as pain creams.” Id. ¶ 78. The marketers received a commission for referrals that they generated. Id. “Schuster, Rall, Zeutzius, and Quintan sought out TRICARE referrals” because of their “high reimbursements.” Id. Neither Schuster, Rall, Zeutzius, nor Quintan were physicians or registered healthcare providers. Id. ¶ 77. On May 1, 2015, TRICARE changed its screening process for compound drug claims, which

resulted in TRICARE paying fewer compound drug claims. Id. ¶ 79. As a result of this change, 1 The Court draws the following factual account from the Government’s Complaint (Doc. 1). 2 “‘Qui tam’ is an abbreviation for qui tam pro domino rege quam pro se ipso in hac parte sequitur, which means ‘who as well for the king as for himself sues in this matter.’” United States ex rel. Grubbs v. Kanneganti, 565 F.3d 180, 184 n.5 (5th Cir. 2009) (quoting Black’s Law Dictionary 1262 (7th ed. 1999)). - 2 - “Schuster, Rall, Zeutzius, and Quintan looked towards toxicology and [pharmacogenomic] tests as a potential source of revenue.” Id. ¶ 80. Pharmacogenomic (“PG”) testing tests “for specific genetic variations that may affect the way that individuals react to certain medications.” Id. ¶ 33. Defendant Cockerell owns and serves as president of CDP, a dermatopathology3 lab that opened in or around June 2013. Id. ¶¶ 2, 74. Cockerell emailed Schuster and Quintan on November

10, 2014, about forming a genomics lab premised on Rxpress’s marketing strategy. Id. ¶ 87. The new business enterprise would use the same business model as Rxpress where the “principals used their network of marketers to generate referrals for clinical lab tests” in exchange for a commission to the marketers for the referrals. Id. ¶ 85. Schuster, Rall, Zeutzius, and Quintan formed Progen Lab Systems, LLC (“Progen”) on or around December 9, 2014, but Progen did not have a Clinical Laboratory Improvement Amendments of 1988 (“CLIA”) license that allowed it to perform laboratory tests or a National Provider Identifier (“NPI”) that allowed it to bill TRICARE. Id. ¶¶ 35,

46, 81. Therefore, Cockerell allowed Progen to use CDP’s CLIA license. Id. ¶¶ 88, 93. On or around February 26, 2015, CDP applied to the Centers for Medicare & Medicaid Services (“CMS”) to add toxicology to its CLIA license, but CDP did not inform the center that Progen would perform the testing. Id. ¶ 101. The license addition was approved on May 23, 2015. Id. CDP and Progen entered into a Management Services and Operations Agreement (“MSA”) on March 10, 2015, whereby “Progen would acquire space, equipment, personnel, and supplies for

CDP’s toxicology and genomic testing” and “perform the toxicology and genomic tests for CDP.” Id. ¶ 93. Progen then leased a suite from CDP for its lab space. Id. ¶ 100. The agreement also contained a revenue sharing clause whereby “Progen would receive 80 percent of the net revenues for the 3 Dermatopathology involves the study of cutaneous diseases—usually involving skin samples—at the microscopic level. Id. ¶¶ 74. - 3 - laboratory services, and CDP would keep the remaining 20 percent.” Id. ¶ 95. Significantly, the agreement prohibited either party from “perform[ing] any services in the lab for any patients enrolled in . . . federal or state healthcare programs” and provided that CDP “would not accept reimbursement from federal healthcare programs for Progen’s referrals.” Id. ¶¶ 96–97. Progen also agreed to indemnify and hold harmless CDP for any negligence or misconduct caused by Progen. Id.

¶ 98. Prior to the agreement with Progen, “CDP did not perform PG or toxicology testing” and TRICARE did not represent a “large portion of CDP’s business.” Id. ¶ 75. This would soon change. Despite the language within the MSA, Progen sought referrals from federal healthcare programs and submitted claims using CDP’s CLIA license and NLIA number. Id. ¶ 104. To generate referrals, Progen used requisition forms containing a multitude of lab tests along with a choice to conduct a “Comprehensive Panel.” Id. ¶ 102. Once received, “the samples went to CDP for testing” and insurance programs reimbursed CDP directly. Id. ¶¶ 102, 104. CDP then provided an

“Explanation of Benefits” with CDP’s name to patients. Id. ¶ 102. Many of the federal referrals came from Prolixus Financial, LLC, d/b/a Alcoholism & Drug Addiction Recovery Group, LLC (“ADAR”) through “a scheme to generate lab referrals from soldiers or their family members stationed near Fort Hood.” Id. ¶¶ 105–06. The ADAR scheme consisted of collecting urine and saliva samples in exchange for $50 Wal-Mart gift cards, shipping the samples to Progen for testing, and billing “TRICARE for medically unnecessary toxicology and

DNA cancer screening tests using CDP’s CLIA license and NPI number.” Id. ¶ 115–19. Two of the sales representatives for Rxpress also became marketers for Progen and used ADAR “to generate lab referrals for Progen.” Id. ¶ 109. For one illustrative claim, CDP sought reimbursement from “TRICARE for twenty types of toxicology tests” by ordering an unnecessary “Comprehensive Panel.”

- 4 - Id. ¶¶ 122–23. TRICARE reimbursed CDP for the testing, which paid Progen, which paid the sales representatives for Rxpress, who shared some of their commissions with ADAR. Id. ¶¶ 115, 123. Eventually, ADAR obtained signature stamps from doctors to sign off on the tests provided by beneficiaries who never saw a doctor, never received test results, and never knew of the purpose for the samples. Id. ¶ 117. Because of this scheme, two sales representatives of Rxpress, the owner and

managing partner of ADAR, and the operations manager of ADAR later pleaded guilty to conspiracy to commit healthcare fraud. Id. ¶¶ 107–08, 118, 224–27. The improper claims submitted by CDP were associated with the improper lab tests conducted by the ADAR Group. Id. ¶ 127. Cockerell and CDP learned that Progen was performing services for TRICARE beneficiaries around June 2015. See id.

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United States v. Cockerell Dermatopathology PA, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-v-cockerell-dermatopathology-pa-txnd-2021.