False Claims Act Developments

To learn more about recent developments in False Claims Act litigation and the measures companies may take to reduce FCA exposure, please see the two publications below:

Compliance Programs:  An Answer to the Risks Posed by the False Claims Act, originally published in the August 2011 issue of Metropolitan Corporate Counsel.

Litigating False Claims Act Cases in the First Circuit Post-Blackstone and Amgen, originally  published in the August 29, 2011 issue of Bloomberg Law Reports.

 

 

Falsity And The FCA: The First Circuit's Blackstone And Amgen Decisions (Part II)

In United States ex rel. Hutcheson et al. v. Blackstone Medical, Inc., 2011 WL 2150191 (1st Cir. June 1, 2011), the relator, a former regional sales manager for Blackstone Medical, Inc., filed a qui tam action against the medical device manufacturer alleging that it violated the federal FCA. The relator alleged that Blackstone caused hospitals and physicians to submit materially false claims to Medicare by engaging in a nationwide kickback scheme to induce physicians to use its medical devices in spinal surgeries. The relator further alleged that Blackstone knew this scheme would cause physicians and hospitals to present Medicare with payment claims that contained material misrepresentations. According to the relator, both hospital and physician claims for reimbursement were allegedly tainted by kickbacks provided to physicians (even though the hospitals were unaware of the kickbacks). The hospitals and physicians who submitted the claims to Medicare were not named as defendants in the action. Blackstone did not submit claims for reimbursement to Medicare. The government declined to intervene in the action (which is typically a sign that the merits of the relator’s claims are weak, the potential damages are low, or both). Blackstone moved to dismiss the action for failure to state a claim under Rule 12(b)(6). At issue was whether the claims were materially false under the FCA.

The Massachusetts district court applied the traditional falsity analysis outlined in Part I and held that the relator’s complaint failed to identify any materially false claims. The First Circuit reversed the district court, rejecting what it deemed to be “judicially created” “categorical rules” to determine whether a claim is materially false under the FCA. According to the First Circuit, the “district court appeared to employ the concept of certification such that a claim can be false or fraudulent only if the submitting entity knew or should have known of the underlying falsehood or fraudulence.” Blackstone, at *10. The First Circuit held that this view was incorrect because “[t]he Supreme Court has long held that a non-submitting entity [such as Blackstone] may be liable under the FCA for knowingly causing a submitting entity [such as the hospitals] to submit a false or fraudulent claim, and it has not conditioned this liability on whether the submitting entity knew or should have known about a non-submitting entity’s lawful conduct.” Blackstone, at * 11. In response to Blackstone’s concerns that failing to adopt the traditional framework for analyzing falsity would overextend liability under the FCA, the First Circuit held that this concern does not “call for ‘adopting a circumscribed view of what it means for a claim to be false or fraudulent,’ but rather calls for ‘strict enforcement of the Act’s materiality and scienter requirements.’” Blackstone, at *9 (quoting United States v. Sci. Applications Int’l Corp., 626 F.3d 1257, 1269 (D.C. Cir. 2010)).

The First Circuit held that the appropriate test for falsity is to determine, without any categorical limitations, whether the claims at issue “misrepresented compliance with a precondition of payment so as to be false or fraudulent,” and if so, “whether those misrepresentations were material.” Blackstone, at *13. The first step of this analysis is to identify a precondition of payment under the relevant government program. In Blackstone, the relator asserted that compliance with the AKS is a precondition of payment under the Medicare program and identified four potential sources to support her argument: (1) the language and legislative history of the AKS; (2) a non-retroactive 2009 amendment to the FCA which provides that violations of the AKS are also violations of the FCA; (3) the hospitals’ Medicare Cost Reports drafted by CMS; and (4) the hospitals’ and physicians’ Medicare Provider Agreements, also drafted by CMS. The First Circuit held that the Medicare Hospital Cost Reports and Provider Agreements established that AKS compliance is a precondition of Medicare payment for the hospital and physician claims at issue. The First Circuit declined to rule on whether the first and second sources established the same.

According to the First Circuit, the Medicare Provider Agreements executed by the hospitals and physicians established that compliance with the AKS is a precondition of payment under Medicare:

The Provider Agreement, drafted by CMS, requires that hospitals and physicians acknowledge that they “understand that payment of a claim by Medicare is conditioned upon the claim and the underlying transaction complying with Medicare’s laws, regulations and program instructions.” The Agreement specifically identifies “the Federal anti-kickback statute” as one of only two enumerated examples of the relevant “laws, regulations, and program instructions.” This language make clear that the federal Medicare program will not pay claims if the underlying transaction that gave rise to the claim violated the AKS. The Agreement makes no exception for instances in which that “underlying transaction” violated the AKS because of the actions of a third party like Blackstone.

Blackstone, at *13.

The First Circuit held that the Medicare Cost Reports submitted by the hospitals likewise demonstrated that AKS compliance is a precondition of Medicare payment:

The Hospital Cost Report, also drafted by CMS, further underscores that hospitals submitting claims represent compliance with the AKS. The form states that “if services identified in this report [were] provided or procured through the payment directly or indirectly of a kickback…fines and/or imprisonment may result.” It also requires that the hospital’s representative sign a statement certifying that he or she is “familiar with the laws and regulations regarding the provisions of health care services, and that the services identified in this cost report were provided in compliance with such laws and regulations.” This makes it abundantly clear that AKS compliance is a precondition of Medicare payment and makes no exceptions for violations caused by third parties like Blackstone.

Blackstone, at *14.

The First Circuit next considered whether compliance with the AKS is a “material” precondition of payment under the Medicare program. Blackstone, at *14-15. Blackstone argued that AKS compliance is irrelevant to the payment of the Medicare claims at issue because neither hospitals nor physicians billed Medicare specifically for Blackstone’s devices. For hospital claims, Blackstone argued that hospitals classified patients within “diagnostic-related groups” (“DRGs”) and received a set payment for treating patients in a group regardless of the particular services provided. For physician claims, Blackstone contended that physicians billed Medicare for their services in performing medically necessary surgeries, not for the devices used because of the alleged kickbacks. The First Circuit declined to adopt Blackstone’s position as a matter of law, and held that the relator’s allegations were “sufficient to show, for purposes of this motion to dismiss, that the kickbacks were capable of influencing Medicare’s decision as to whether to pay the hospital and physician claims.” Blackstone, at *15. The First Circuit observed that “[e]xpress contractual language may ‘constitute dispositive evidence of materiality,’ but materiality may be established in other ways, ‘such as through testimony demonstrating that both parties to the contract understood that payment was conditional on compliance with the requirement at issue.’” Blackstone, at 15.

Based on this analysis, the First Circuit reversed the district court’s dismissal of the relator’s complaint under Rule 12(b)(6) for failing to identify a materially false claim under the federal FCA, and remanded the action.

Tomorrow, we will discuss the First Circuit’s application of its new falsity analysis to the state FCA claims at issue in New York ex rel. Westmoreland et al. v. Amgen, Inc. et al.

Falsity And The FCA: The First Circuit's Blackstone And Amgen Decisions (Part I)

The False Claims Act does not define what types of claims are “false.” Consequently, one of the key battles at the motion to dismiss stage in FCA litigation is whether the conduct alleged by the plaintiff can give rise to a “false” claim as a matter of law. For the past decade, courts addressing this issue have held that the FCA recognizes two categories of actionable false claims – factually false claims and legally false claims. Courts have also recognized that there are at least two subcategories of legally false claims – express certification claims and implied certification claims. A factually false claim is one that involves an incorrect description of goods or services provided or a request for reimbursement for goods or services never provided. A legally false claim is one that is not factually false (i.e., not false on its face), but is false for an extrinsic legal, regulatory or contractual reason; for example, by incorrectly certifying compliance (either expressly or impliedly) with a statute, regulation, or contractual obligation that is a prerequisite to government payment.

In a pair of recent cases, the First Circuit held that this categorical framework for determining falsity is too restrictive and rejected it. See United States ex rel. Hutcheson et al. v. Blackstone Medical, Inc., 2011 WL 2150191 (1st Cir. June 1, 2011); New York ex rel. Westmoreland et al. v. Amgen, Inc. et al., 2011 WL 2937420 (1st Cir. July 22, 2011). In doing so, the First Circuit observed that “[t]he text of the FCA does not refer to ‘factually false’ or ‘legally false’ claims, nor does it refer to ‘express certification’ or ‘implied certification.” Blackstone, at *7. The First Circuit reasoned that “[j]udicially-created categories sometimes can help carry out a statute’s requirements, but they can also create artificial barriers that obscure and distort those requirements.” Blackstone, at *7. According to the First Circuit, “in enacting the FCA, ‘Congress wrote expansively, meaning to reach all types of fraud, without qualification, that might result in financial loss to the Government.’” Blackstone, at *12. 

In the First Circuit’s view, the appropriate test to determine falsity under the FCA is a “fact-intensive” and “context-specific” inquiry into whether the claims presented to the government misrepresented that there had been compliance with a material precondition of payment recognized by the particular government program at issue. Amgen, at *6; Blackstone at *13.  In Blackstone, which involved the federal FCA, the First Circuit applied this new falsity test to claims allegedly tainted by kickbacks under the federal Medicare program. In Amgen, which involved analogous state FCAs in New York, Massachusetts, California, Georgia, Illinois, Indiana, and New Mexico, the First Circuit applied the new test to allegedly kickback tainted claims under the state Medicaid programs in those seven states.

This week, we are publishing a series a posts discussing the First Circuit’s recent Blackstone and Amgen decisions. Parts II and III will examine the application of the First Circuit’s new falsity test to the claims at issue in the Blackstone and Amgen cases. Part IV will explore the potential consequences of the First Circuit’s new falsity test and will suggest measures companies may want to consider to minimize FCA exposure. Part V will discuss why, and how, the U.S. Supreme Court should resolve the circuit split created by the First Circuit.

Public Disclosures in Civil Complaints and Media Bar Relator's Action

In United States ex rel. Poteet v. Bahler Medical, Inc., No. 09-1728, 2010 WL 3491159 (1st Cir. Sept. 8, 2010), the First Circuit affirmed the dismissal of a relator’s qui tam action.  The relator brought the action against 120 spine surgeons and 18 medical device distributors, making allegations surrounding the promotion of a medical device manufactured by Medtronic to third-party doctors allegedly knowing that the third-party doctors would submit false claims for reimbursement.  The First Circuit affirmed the District Court’s holding that the claims against the doctors were jurisdictionally barred by the FCA’s “public disclosure bar” because the alleged fraud was publicly disclosed in civil complaints against Medtronic and various doctors and in the related media coverage.

Section 3730(e)(4)(A) of the FCA provides that no court shall have jurisdiction over an FCA action brought by a relator that is based on prior public disclosures of fraud.  The First Circuit held that “[t]o be a disclosure ‘of fraud’ the disclosure must contain either (1) a direct allegation of fraud, … or (2) both a misrepresented state of facts and a true state of facts so that the listener or reader may infer fraud.”  The Court also held that the public disclosures must be from the “statutorily specified sources,” which include “civil…hearing” and “news media.”

There was no dispute that civil complaints filed in state and federal court contained the direct allegations of fraud.  The relator argued, however, that civil complaints did not qualify as public disclosures under the FCA.  The First Circuit rejected this argument, holding that, for purposes of this provision of the FCA, “hearing” is synonymous with “proceeding,” and thus, civil complaints fall within the statutorily specified public disclosures.  The First Circuit also rejected the argument that civil complaints filed in state court as opposed to federal court should not qualify as public disclosures.  The public disclosure bar, therefore, deprived the court of jurisdiction.

The relator did not claim to be an “original source” of information, so this exception to the public disclosure bar did not apply.  Additionally, the First Circuit held that, though a case dismissed for lack of subject matter jurisdiction is usually without prejudice since it is not on the merits and jurisdictional defects may be cured, in this case, the jurisdictional defect was incurable, and thus, the case is “forever barred.”

This case was decided under the version of the FCA’s public disclosure bar in effect prior to its amendment by the Patient Protection and Affordable Care Act (PPACA).  The First Circuit noted that the PPACA’s addition of the term “Federal” before “criminal, civil, or administrative hearing” means that civil complaints filed in state court no longer qualify as public disclosures under the FCA.  In other words, according to the First Circuit, a relator may not be barred from bringing an FCA Action where the fraud was previously publicly disclosed in an action filed in state court. 

First Circuit Vacates Jury Verdict Based on Exclusion of Materiality Evidence

In United States ex rel. Loughren v. Unum Group, Case No. 09-1606, 2010 WL 2951175 (1st Cir. July 29, 2010), the First Circuit vacated a jury verdict and remanded the case for a new trial because the District Court improperly excluded evidence relevant to the materiality element of the FCA. The relator alleged that Unum Group, a long-term disability insurer, caused claimants to submit false claims for Social Security Disability Insurance (SSDI) by requiring them to apply for SSDI benefits in order to receive long-term disability benefits from Unum. The Government did not intervene in this action. 

Unum’s requirements to qualify for disability benefits were less stringent than that of the Social Security Administration (SSA). An applicant needed only to show that he or she is unable to work in his or her “own occupation.”  By contrast, to obtain SSDI benefits, the applicant must show that he or she cannot engage in any “substantial gainful activity.” In other words, a person may qualify for benefits from Unum, but not SSDI benefits. The SSDI application inquires when the applicant has been “unable to work,” i.e., “inability to engage in any substantial gainful activity.” This question must be answered affirmatively to apply for SSDI benefits. The relator alleged that, since the applicants were required by Unum to apply for SSDI benefits, and thus answer this question affirmatively, Unum caused certain applicants to make false statements in their SSDI applications. 

The District Court held, and the First Circuit agreed, that liability under the FCA requires that the false statements be material. Following the Fourth, Fifth and Ninth Circuits, as well as the recent definition incorporated into the FCA by the Fraud Enforcement and Recovery Act (FERA), the First Circuit held that materiality under the FCA, pre and post-FERA, means that the false statement has “a natural tendency to influence, or is capable of influencing,” the Agency’s decision whether or not to award SSDI benefits. The test does not require that the false statement actually influence the Agency’s decision, only that it is capable of influencing it. Unum sought to introduce evidence at trial that, like Unum’s policy, the federal government, under the Federal Employee Retirement System (FERS), required all claimants to apply for SSDI benefits. Unum further sought to present evidence that the Social Security Administration (SSA) was aware of this practice and that the SSA did not differentiate between FERS applicants and Unum applicants. The District Court excluded this evidence. The First Circuit held, however, that the evidence supports Unum’s defense that the answer to the question in the SSDI application regarding when the claimant is “unable to work” is not material, i.e., not capable of influencing the agency’s decision, because, in light of the FERS evidence, a jury could reasonably conclude that the SSA had no reason to believe that any applicant may be entitled to benefits by affirmatively responding to this question. 

Typically, courts have considered government knowledge defenses in the context of the elements of "falsity" and "scienter."  In this case, the First Circuit considered government knowledge with respect to the materiality element of the FCA.  Based on the First Circuit's decision, the government's knowledge and practices can preclude a plaintiff from establishing the materiality element of an FCA claim.  

Supreme Court Denies Certiorari on "Original Source" Question

On June 21, 2010, the U.S. Supreme Court denied certiorari in Ortho Biotech Products, L.P. v. United States ex rel. Duxbury, No. 09-654, 2010 U.S. LEXIS 5091, thereby  allowing a circuit split to continue on a question relating to the jurisdiction over a relator’s action. The Government did not intervene in this action, so this action was litigated solely by the relator. Under the FCA, where there has been a public disclosure of the allegations, the court only has jurisdiction over a relator’s action if the relator is an “original source” of the information and voluntarily provided the information to the Government. 

The circuits have been split on whether this requirement means that the relator was required to provide the information to the Government before the “public disclosure” or simply before filing the lawsuit. In United States ex rel. Duxbury v. Ortho Biotech Products, L.P., 579 F.3d 13 (1st Cir. 2009), the First Circuit joined the Fourth and Eighth Circuits in holding that a relator need only provide information to the Government before filing suit, and not before the public disclosure. By contrast, the Sixth and DC Circuits have held that an “original source” must provide the Government with the information prior to any public disclosure. The Second and Ninth Circuits have adopted an even stricter requirement, holding that a relator must actually be the source of the public disclosure.

Congress recently amended the FCA’s “original source” provision in the Patient Protection and Affordable Care Act (PPACA), Pub. L. No. 111-148, 124 Stat. 119 (Mar. 23, 2010). The PPACA provides that a person qualifies as an “original source” if the person either: (a) voluntarily discloses the information to the Government “prior to a public disclosure,” or (b) voluntarily discloses the information to the Government before filing an action and “has knowledge that is independent of and materially adds to the publicly disclosed allegations.” However, this provision of the PPACA is not retroactive, see Graham County Soil & Water Conservation Dist. v. United States ex rel. Wilson, 130 S. Ct. 1396, 1400 n. 1 (2010), and thus, the Duxbury question and the circuit split will continue to have practical significance for cases that will be decided under the prior version of the FCA.