United States of America v. Barton & Associates, Inc.

CourtDistrict Court, D. Massachusetts
DecidedMarch 29, 2024
Docket1:20-cv-11231
StatusUnknown

This text of United States of America v. Barton & Associates, Inc. (United States of America v. Barton & Associates, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States of America v. Barton & Associates, Inc., (D. Mass. 2024).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MASSACHUSETTS

CIVIL ACTION NO. 20-11231-GAO

UNITED STATES OF AMERICA, et al., ex rel. REYNALDO SOLANO and NEALS MAXILIN, Plaintiffs,

v.

BARTON & ASSOCIATES, INC., MEDTECH WORLDWIDE, INC., REALTIME PHYSICIANS, LLC, OCENTURE, LLC, and CARELUMINA, LLC, Defendants.

OPINION AND ORDER March 29, 2024

O’TOOLE, D.J. This is a qui tam action brought in 2020 by Relators Reynaldo Solano and Neals Maxilin on behalf of the United States and several States pursuant to the False Claims Act (the “FCA”) and analogous state statutes. The relators allege that Barton & Associates, Inc. knowingly either provided or contracted with providers to furnish unnecessary medical services and equipment to patients eligible for Medicare or other government-funded health plans. The United States declined to intervene, and the defendant Barton subsequently moved to dismiss. I. Overview of Allegations The complaint alleges that Barton provides “locum tenens” staffing services, assigning physicians, physician assistants, dentists, and other health care workers to short- and long-term positions at hospitals and health care organizations across the country. The relators claim that Barton physicians knowingly prescribed unnecessary medical services and equipment. The relators' complaint alleges that Barton recruits individuals or entities to obtain contact information of patients eligible for Medicare or other government-funded health plans.1 Barton then encourages the recruited client to establish a call center to solicit eligible patients for services such as genetic cancer screening, durable medical equipment, pain creams, anti-fungal creams, and hydrotherapy foot soaks. Once a Medicare-eligible patient is identified, the recruited client can forward the patient’s information to Barton, which then assigns the matter to one of its own physicians to

prescribe the service or product. The physician must review the request, but almost all requests are approved. Barton then collects an assessment fee of forty dollars for each item or service, while the recruited client obtains reimbursement from Medicare. The complaint further alleges that Medtech Worldwide Inc. (“Medtech”) and RealTime Physicians, LLC (“RealTime”), two operators of a network of virtual medical clinics, were among the clients Barton recruited and for whom Barton physicians provided unnecessary prescriptions. The recruited clients obtained “tens of thousands” of dollars in prescriptions every month for genetic testing, durable medical equipment, and pain cream prescriptions from Barton physicians and then sought reimbursement for those prescriptions. (Compl. ¶ 60 (dkt. no. 1).) For example,

on January 10, 2019, Barton was asked to generate a prescription for genetic testing for a patient. A Barton-contracted physician signed the prescription without ever meeting, seeing, or communicating with the patient. Similarly, CareLumina LLC, a telehealth company, and its owner, Ocenture LLC, also contracted with Barton to obtain prescriptions for unnecessary services and equipment. The two companies offered no-cost testing for cancer markers and contracted with Barton to obtain signed prescriptions for the tests so that they could bill Medicare. They performed between 8,000 and 10,000 cancer-screening tests per month.

1 For the sake of brevity, this order hereinafter will refer only to Medicare, but the allegations in the complaint typically refer to “Medicare or other government funded health plans.” II. Discussion The relators rely on many of the provisions of the FCA to target allegedly false claims, including the presentation of false claims under 31 U.S.C. § 3729(a)(1)(A) (Count I), making or using a false record or statement to cause claims to be paid under § 3729(a)(1)(B) (Count II), conspiracy to commit a violation under § 3729(a)(1)(C) (Count III), knowingly delivering less

than all of the government’s property in Barton’s possession under § 3729(a)(1)(D) (Count IV), and knowingly concealing or improperly avoiding an obligation to pay money to the government under § 3729(a)(1)(G) (Count V). They further allege violations of the California, Florida, Illinois, Massachusetts, Michigan, New Jersey, New York, and Texas state false claims acts (Count VI through XIII). A. The False Claims Act The FCA penalizes those who present, or cause to be presented, “false or fraudulent claim[s] for payment or approval” to the federal government. 31 U.S.C. § 3729(a)(1). Thus, fraud under the FCA has two components: the defendant must submit or cause the submission of a claim for payment to the government, and the claim for payment must itself be false or fraudulent. United States ex rel. Ge v. Takeda Pharm. Co., 737 F.3d 116, 124 (1st Cir. 2013) (“Because FCA liability attaches only to false claims, merely alleging facts related to a defendant’s alleged misconduct is not enough. Rather, a complaint based on [the FCA] must sufficiently establish that false claims were submitted for government payment as a result of the defendant’s alleged misconduct.”) (internal citations omitted). Federal Rule of Civil Procedure 9(b), meanwhile, requires that a complaint state these components with “particularity,” meaning relators . . . must allege the “who, what, when, where, and how of the alleged fraud.” Id. at 123 (internal citation and quotation marks omitted). Still, we have repeatedly emphasized that there is no “checklist of mandatory requirements” that each allegation in a complaint must meet to satisfy Rule 9(b), United States ex rel. Karvelas v. Melrose–Wakefield Hosp., 360 F.3d 220, 233 (1st Cir. 2004), abrogated on other grounds by U.S. ex rel. Gagne v. City of Worcester, 565 F.3d 40, 46 n.7 (1st Cir. 2009), and that a “somewhat ‘more flexible’ standard” applies in qui tam actions where the defendant is alleged to have induced third parties to file false claims, United States ex. rel. Kelly v. Novartis Pharms. Corp., 827 F.3d 5, 13 (1st Cir. 2016) (quoting United States ex rel. Duxbury v. Ortho Biotech Prod., L.P., 579 F.3d 29–30 (1st Cir. 2009)). Hagerty ex rel. United States v. Cyberonics, Inc., 844 F.3d 26, 31 (1st Cir. 2016). As explained in Hagerty, there is a “distinction between a qui tam action alleging that the defendant made false claims to the government,” and a case, where “the defendant induced third parties to file false claims with the government,” what is at issue in this case. Duxbury, 579 F.3d at 29. Relators alleging inducement “can meet this more accommodating standard by ‘providing

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United States of America v. Barton & Associates, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-of-america-v-barton-associates-inc-mad-2024.