United States v. AIMA Business and Medical Support, LLC

CourtDistrict Court, S.D. Florida
DecidedSeptember 17, 2025
Docket1:25-cv-22507
StatusUnknown

This text of United States v. AIMA Business and Medical Support, LLC (United States v. AIMA Business and Medical Support, LLC) is published on Counsel Stack Legal Research, covering District Court, S.D. Florida primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States v. AIMA Business and Medical Support, LLC, (S.D. Fla. 2025).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF FLORIDA

CASE NO. 25-22507-CIV-ALTONAGA/Reid

UNITED STATES OF AMERICA,

Plaintiff, v.

AIMA BUSINESS AND MEDICAL SUPPORT, LLC,

Defendant. ________________________________/ ORDER

THIS CAUSE came before the Court on Defendant, AIMA Business and Medical Support, LLC’s Motion to Dismiss Plaintiff’s Complaint [ECF No. 14], filed on August 5, 2025. Plaintiff, the United States of America (“the Government”) filed a Response [ECF No. 17]; to which Defendant filed a Reply [ECF No. 18]. The Court has reviewed the Complaint [ECF No. 1], the parties’ written submissions, and applicable law. For the following reasons, the Motion is denied. I. BACKGROUND

This False Claims Act (“FCA”) case arises from allegations that Defendant submitted thousands of Medicare claims for genetic laboratory tests that were not medically necessary, not ordered by a treating physician, and not prescribed for the diagnosis or treatment of an illness or injury. (See generally Compl.). Selecta Laboratory (“Selecta”) is a Miami-based laboratory. (See id. ¶ 15). In May 2018, Selecta changed owners: Richard Luzzi and Jamie Nocher bought the company and became its managers in May 2018, despite having no background in medicine. (See id. ¶¶ 65–68). Several months later, in July 2018, Selecta hired Defendant — a business-process outsourcing company based in the United Kingdom and India — to handle Medicare billing, provide Medicare billing guidance, and keep Selecta updated on Medicare guidelines. (See id. ¶¶ 2, 11, 14, 79–81). Medicare reimburses only for services that are “reasonable and necessary for the diagnosis or treatment of illness or injury[.]” (Id. ¶ 53 (quoting 42 U.S.C. § 1395y(a)(1)(A) (alteration added;

other citation omitted)). Diagnostic testing is covered only when necessary for such a purpose and ordered by a beneficiary’s treating physician. (See id. ¶ 56 (citing 42 C.F.R. § 410.32)). Generally, Medicare does not cover genetic tests performed for informational or screening purposes. (See id. ¶ 55 (citing 42 C.F.R. § 411.15(a)(1)). Notwithstanding these restrictions, Defendant sent Luzzi and Nocher sample Explanation of Benefits (“EOBs”) for genetic lab testing, indicating Selecta could make a substantial profit by billing Medicare for cancer genomic (“CGx”) and pharmacogenomic (“PGx”) tests for patients having a personal history of cancer. (See id. ¶¶ 80–87, 89). Defendant advised Selecta it could obtain the highest Medicare reimbursements for genetic tests for Lynch syndrome and breast and ovarian cancer. (See id. ¶¶ 90, 93 (“If you have noticed, your breast and ovarian panel pays better

than multiple cancer panel . . . . It is advisable to request physicians to order breast and ovarian panel if possible.” (alteration added; emphasis omitted))). Following Defendant’s advice, Selecta began using telemarketers who did not have medical backgrounds to convince Medicare beneficiaries to undergo CGx and PGx genetic tests that would be “paid for by Medicare” at “no out-of-pocket cost[.]” (Id. ¶ 69 (alteration added; quotation marks omitted); see also ¶ 70). When beneficiaries agreed to testing, Selecta “sent notaries or agents” to swab them for their DNA “without a doctor’s order and with no medical supervision or direction[.]” (Id. ¶ 123 (alteration added)). Selecta also retained “telemedicine” doctors, who reviewed and signed the telemarketers’ call notes in an electronic portal and signed corresponding Medicare billing forms. (Id. ¶ 124 (quotation marks omitted)). On September 26, 2018, with the telemarketing campaign underway, Luzzi emailed Defendant a link to a Centers for Medicare & Medicaid Services website page adressing Medicare

coverage for laboratory services. (See id. ¶ 126). Defendant responded the next day, stating: The below mentioned link doesn’t say anywhere that sample can be collected before the physician visit, but it clearly says that medical necessity documentation when ordering for a laboratory test is essential and it has to be clearly mentioned in the progress notes or signed visit office note, this clearly means that a doctor has to screen the patient and the notes of the doctor should mention the necessity of the Laboratory test, [sic] In that scenario if the sample was collected earlier and patient goes to a doctor [sic] gets the documents signed later [sic] is completely not logical and illegal.

We can suggest 2 ways, i.e. the doctor notes should be on the sample collection date or the notes shouldn’t consist of any date information when the doctor did the screening.

(Id. ¶ 127 (emphasis adopted)). After sending the email, Defendant continued submitting claims to Medicare on behalf of Selecta for genetic testing — reviewing and approving the telemedicine doctors’ notes and letters regarding the medical necessity of the genetic tests and submitting bills to Medicare. (See id. ¶¶ 111, 130). Defendant’s work led to a significant increase in Selecta’s Medicare billing. (See id. ¶¶ 63–64). Before 2018, Selecta did not bill Medicare for genetic tests and only billed a minimal number of other tests to Medicare. (See id. ¶ 63). Between August 22, 2018 and August 13, 2019, Selecta billed Medicare approximately $15,178,946.00 for genetic tests. (Id. ¶ 64). On January 28, 2019, Selecta was notified it had been placed on pre-payment benefit integrity review after an audit indicated an alarming number of Selecta’s submissions did not adhere to Medicare’s requirements for billing for genetic testing. (See id. ¶¶ 133–135). Selecta informed Defendant about the benefits integrity review, and Defendant helped Selecta respond — while continuing to bill for the same genetic tests, using the same telemarketing practices and doctor-review system. (See id. ¶¶ 136–140). Defendant and Selecta also discussed billing for genetic tests in a different Medicare region “that might continue paying for the fraudulent genetic tests” while the review was underway. (Id. ¶ 141; see also id. ¶ 142).

The Government brings four claims for relief: violation of the FCA, 31 U.S.C. section 3729(a)(1) (“Count I”) (see id. ¶¶ 164–69); violation of the FCA, 31 U.S.C. section 3729(a)(1)(B) (“Count II”) (see id. ¶¶ 170–76); and two common-law claims — unjust enrichment and payment by mistake (“Counts III–IV”) (see id. ¶¶ 177–83). Defendant moves to dismiss the Complaint, arguing that Counts I–II are “shotgun pleadings” that do not meet Federal Rule of Civil Procedure 9(b)’s particularity standard, and each count should be dismissed as insufficiently pleaded under Rule 12(b)(6). (See generally Mot.). II. LEGAL STANDARDS

Rule 12(b)(6). “To survive a motion to dismiss [under Federal Rule of Civil Procedure 12(b)(6)], a complaint must contain sufficient factual matter, accepted as true, to ‘state a claim to relief that is plausible on its face.’” Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009) (alteration added; quoting Twombly, 550 U.S. at 570). Although this pleading standard “does not require ‘detailed factual allegations,’ . . .

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