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DOJ Follows Through on a 2018 New Years’ Resolution: Rein In Qui Tam Actions

Along with most of us, last January DOJ set its own goals for 2018: new policies related to False Claims Act (“FCA”) enforcement. One such “resolution” for 2018 was the DOJ Civil Fraud section’s  instruction to its attorneys and all AUSAs handling FCA cases to routinely consider whether declined qui tam actions should be dismissed under the Department’s authority in Section 3730(c)(2)(A) of the FCA, which it had rarely used from 1986 through 2017. Known as the “Granston Memo” (which we discuss here) and now codified in the Justice Manual, the central theme of the instruction is that seeking dismissal of qui tam actions may be in the government’s interest  to “preserve limited resources and avoid adverse precedent.” 

Throughout the year, we tracked DOJ’s use of this authority, and DOJ did seem to be seeking dismissals more frequently in district court cases when it was not in the federal interest for litigation to proceed.  But the end of 2018 brought two dramatic developments.  As we discussed previously, in response to the Supreme Court’s request for the Solicitor General’s views on a certiorari petition in a Ninth Circuit case regarding the “materiality” standard, the Solicitor General declared that it agreed with the relator that materiality had been adequately pleaded but that, if remanded, DOJ would exercise its dismissal authority under the FCA.

Then, this week, DOJ filed motions in district courts seeking to dismiss eleven declined cases, filed in seven different jurisdictions, and involving thirty-eight different defendants. The cases involve a theory of liability under the FCA that pharmaceutical assistance services provided by manufacturers to patients and their physicians regarding the proper administration of drugs and related support are actually illegal promotional activity or “white coat marketing” and therefore unlawful kickbacks. The cases were clones of each other, and were filed by an LLC formed for the purpose of filing these actions. DOJ asserted that dismissal is appropriate on the basis of the governmental purposes of “preserving scarce government resources” and “protecting important policy prerogatives of the federal government’s healthcare programs.” DOJ also stated that it extensively investigated the complaints, and concluded that the allegations lack sufficient factual and legal support.

DOJ, in these motions, indicated in some more detail the programmatic reasons why it is not in the federal government’s interest for the cases to proceed:

These relators should not be permitted to indiscriminately advance claims on behalf of the government against an entire industry that would undermine common industry practices the federal government has determined as, in this particular case, appropriate and beneficial to federal healthcare programs and their beneficiaries.

Of note, DOJ’s position is that the legal standard should be the one articulated in the D.C. Circuit’s opinion in Swift v. United States, 318 F.3d 250, 252 (D.C. Cir. 2003), which is that United States has “unfettered discretion” to dismiss cases under its authority in Section (c)(2)(A).  But DOJ also notes that under the alternative standard established in United States ex rel. Sequoia Orange Co. v. Baird-Neece Packing Corp., 151 F.3d 1139 (9th Cir. 1998), which requires a “valid governmental purpose” and a “rational relationship” between dismissal and that purpose, that standard is easily met and the cases should be dismissed.  Under the Swift standard, the district courts would have no role in reviewing DOJ’s reasons for dismissal; under the Sequoia Orange standard, the relator would then have the burden to demonstrate that the dismissal is “fraudulent, arbitrary and capricious, or illegal.”

The purpose of the FCA and its qui tam provisions is to protect the interests of the United States, and remedy instances of fraud involving federal funds.  These actions by DOJ demonstrate DOJ’s commitment to these principles, and to ensuring that litigation brought on behalf of the United States is for the benefit of its programs and Treasury.  Best wishes to DOJ for “unfettered discretion” to dismiss in 2019!

©1994-2020 Mintz, Levin, Cohn, Ferris, Glovsky and Popeo, P.C. All Rights Reserved.National Law Review, Volume VIII, Number 354


About this Author

Laurence J. Freedman, Litigation Attorney, Mintz, Enforcement Defense Law

Larry has a deep understanding of what drives government enforcement actions, and how to defend against them, in the health care and life sciences industries. As a trial lawyer and then official in the Civil Fraud Section of the U.S. Department of Justice, he litigated and supervised hundreds of False Claims Act and qui tam cases nationally. In his litigation practice, Larry has successfully represented hospitals and health care systems, laboratories, pharmaceutical and device manufacturers, and health care executives against fraud and abuse allegations and investigations brought by...

Bridgette A. Keller, health system administration LAWYER, Mintz

Bridgette applies her experience in health system administration and ethics in health care to her health law practice. Bridgette advises health care providers, ACOs, health plans, PBMs, and laboratories on a variety of regulatory, fraud and abuse, and business planning matters.

With a background in health care operations, Bridgette is able to provide clients with practical insight that includes a focus on the business implications of health care enforcement defense activities, internal investigations, regulatory compliance, and fraud and abuse analyses of proposed new procedures.

Bridgette's work also includes a focus on ethics in health care principles. As a health care ethicist with the Department of Veterans Affairs National Center for Ethics in Health Care (NCEHC), Bridgette provided technical guidance on health care ethics problems to VA stakeholders, VA Central Office staff, and field-based consultants. She also collaborated on the development of an ethics consultation program and educational materials. Prior to her appointment at the NCEHC, Bridgette served as the Outpatient Clinic Coordinator at the Manhattan Campus of the VA New York Harbor Healthcare System and completed the Graduate Health Administration Training Program at the Washington DC VA Medical Center. Her health care management experience includes outpatient clinical operations, customer service, performance improvement, program development and implementation, data analysis, and supervision of staff.

Bridgette is trained in Lean/Six Sigma thinking and as an examiner for the Baldrige Criteria for Performance Excellence.