Hagerty Ex Rel. United States v. Cyberonics, Inc.

844 F.3d 26, 96 Fed. R. Serv. 3d 572, 2016 U.S. App. LEXIS 22405, 2016 WL 7321224
CourtCourt of Appeals for the First Circuit
DecidedDecember 16, 2016
Docket16-1304P
StatusPublished
Cited by65 cases

This text of 844 F.3d 26 (Hagerty Ex Rel. United States v. Cyberonics, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the First Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Hagerty Ex Rel. United States v. Cyberonics, Inc., 844 F.3d 26, 96 Fed. R. Serv. 3d 572, 2016 U.S. App. LEXIS 22405, 2016 WL 7321224 (1st Cir. 2016).

Opinion

STAHL, Circuit Judge.

Relator-Appellant Andrew Hagerty (“Hagerty”) brought a qui tam action against Appellee Cyberonics, Inc. (“Cyber- *29 onics”) alleging, among other things, that Cyberonics violated the False Claims Act (“FCA”), 31 U.S.C. § 3729 et seq., and related state statutes. Specifically, Hagerty alleged that Cyberonics promoted medically unnecessary replacements of batteries in nerve stimulator devices used to treat epilepsy patients, which in turn resulted in patients and medical providers filing false claims for reimbursement from government health care programs.

The district court dismissed all but two of Hagerty’s claims under Federal Rule of Civil Procedure 12(b)(6), including the FCA allegations, holding that Hagerty’s First Amended Complaint was not pled with the particularity required by Federal Rule of Civil Procedure 9(b). 1 Following this dismissal, the district court also denied Hagerty’s request for leave to file a Second Amended Complaint on the basis of undue delay. Hagerty now challenges the district court’s ruling on both fronts, maintaining that his First Amended Complaint satisfies Rule 9(b) and asserting that the district court abused its discretion when denying his motion for leave to file a Second Amended Complaint. After careful consideration, we affirm.

I. Facts & Background

We recite the relevant facts as they appear in Hagerty’s First Amended Complaint. See Hochendoner v. Genzyme Corp., 823 F.3d 724, 730 (1st Cir. 2016). The Vagus Nerve Stimulator (VNS) is a medical device that is implanted in patients with refractory epilepsy, a severe form of the disease in which a patient’s seizures seriously interfere with their quality of life and do not respond to other medications or treatment. The VNS works by delivering short electrical pulses to the vagus nerve through a wire. Each VNS system contains a battery, and the entire VNS system must be surgically replaced when the battery nears the end of its life.

Patients with refractory epilepsy often qualify for coverage under government' healthcare programs like Medicare and Medicaid. Some treatments for refractory epilepsy, including placement of the VNS, are reimbursed by those programs. These programs impose certain requirements on healthcare providers, such as signing a Provider Agreement with the Centers for Medicare and Medicaid Services (“CMS”). In these agreements, providers certify, among other things, that their claims for reimbursement relate to a reasonable and medically necessary treatment. 42 U.S.C. § 1395y(a)(l)(A).

On February 4, 2013, Hagerty filed a qui tarn complaint under seal against Cyberon-ics, alleging that it engaged in a fraudulent scheme to encourage doctors and patients to prematurely and unnecessarily replace batteries in VNS systems. Hagerty, having gained knowledge of the scheme firsthand as a former sales representative of Cyber-onics, further alleged that this scheme caused significant monetary damages to government healthcare programs by inducing patients and medical providers to file false claims for reimbursement in violation of 31 U.S.C. § 3729(a). On October 29, 2013, the government filed a notice declining to intervene in the case, and on December 5, 2013 the complaint was unsealed and served on Cyberonics. Cyberonics then moved to dismiss the complaint on *30 April 28, 2014 on several grounds, including under Rule 12(b)(6) for failure to state a claim and Rule 9(b) for failure to allege instances of fraud with particularity.

Hagerty amended his pleadings and filed his First Amended Complaint on May 19, 2014. The First Amended Complaint alleged that in 2005, the FDA approved the VNS as a treatment for depression, and, anticipating that much of its future growth would come from this market, Cy-beronics hired 300 new salespersons. Cy-beronics then allegedly began lobbying CMS to approve Medicare reimbursement for VNS therapy in depressive patients, which CMS ultimately declined to grant. Facing a dire financial situation 2 , Cyberon-ics reportedly decided to refocus its sales efforts on epilepsy patients, with a particular interest in re-sales to already existing VNS patients.

The First Amended Complaint emphasized that this new sales plan was driven by a “carrot and stick” approach, where sales representatives were rewarded for meeting “aggressive sales quotas,” were placed in a Performance Improvement Program if they did not achieve 75% of their revenue goals in a given quarter, and were terminated the following quarter if their performance did not improve. Hagerty alleged that, under such conditions, Cy-beronics’ sales representatives resorted to fraudulent sales tactics, such as refusing to provide doctors and patients with accurate VNS battery life calculations and encouraging doctors and patients to replace these batteries prematurely. 3

The First Amended Complaint further alleged that approximately 50% of Cyber-onics’ revenue came from Medicare and Medicaid, with additional revenues coming from TRICARE, the Department of Defense, the Department of Veterans Affairs, and the Federal Employee Health Benefits Program. Hagerty went on to list sixteen hospitals which he claimed had performed and billed for VNS therapy implants in epileptic patients, and specifically named the Southbury Training School, Monson Development • Center, and Wrentham Development Center as “long-term care facilities . ..■ in which vulnerable patients were subjected to unnecessary surgeries to implant replacement devices.” The First Amended Complaint further identified a Dr, Pena, who had three patients undergo battery replacement procedures between September 30, 2010 and November 18, 2010. It also identified a Dr. Thompson, who allegedly, told Hagerty that a Cyber-onics sales representative falsely told physicians to replace VNS batteries prematurely. Moreover, . the First Amended Complaint alleged that Hagerty reviewed an internal patient list and saw that several of Dr. Thompson’s patients had received VNS device replacements in 2010..

By way of conclusion, the First Amended Complaint projected that at least 10,000 medically unnecessary VNS device replacements had occurred at these hospitals and centers since 2007. Coupled with an estimated cost of $20,000 per procedure and an assumption that government healthcare programs covered approximately 50-60% of these procedures, Hagerty reasoned that government healthcare programs lost at least $100 million as a result of Cyberonics’ scheme,

Cyberonics again moved to' dismiss the case. On March 31, 2015, the district court *31

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844 F.3d 26, 96 Fed. R. Serv. 3d 572, 2016 U.S. App. LEXIS 22405, 2016 WL 7321224, Counsel Stack Legal Research, https://law.counselstack.com/opinion/hagerty-ex-rel-united-states-v-cyberonics-inc-ca1-2016.