Explaining Qui Tam Law "qui tam is a writ through which private individuals who assist a prosecution can receive for themselves all or part of the damages or financial penalties recovered by the government as a result of the prosecution. Its name is an abbreviation of the Latin phrase qui tam pro domino rege quam pro se ipso in hac parte sequitur, meaning "[he] who sues in this matter for the lord king as well as for himself."
Qui tam is a legal mechanism derived from the Latin phrase "qui tam pro domino rege quam pro se ipso in hac parte sequitur," which translates to "he who sues in this matter for the king as well as for himself." It allows private individuals, known as relators or whistleblowers, to file lawsuits on behalf of the government against entities or persons who have defrauded the government. In return, the relator may receive a portion of any financial recovery. This provision encourages citizens to expose fraud that might otherwise go undetected, especially in areas like government contracting, healthcare, and defense, where public funds are at stake. Qui tam actions are a form of public-private partnership in law enforcement, rooted in ancient legal traditions but most prominently codified in modern statutes like the U.S. False Claims Act (FCA).
- 18 U.S.C. § 962: Arming vessels against friendly nations.
- 25 U.S.C. § 201: Violations of Indian protection laws.
- 46 U.S.C. § 80103: Removing undersea treasure from Florida to foreign nations.
- 35 U.S.C. § 292: False patent marking (qui tam provision removed in 2011 after being ruled unconstitutional in some cases).
- Filing the Complaint: A relator with direct knowledge of fraud files a lawsuit under seal in federal court, serving it on the government but not the defendant. The complaint must detail the fraud allegations. The seal allows the government time to investigate without alerting the defendant, though this can conflict with securities laws requiring disclosure of material lawsuits.
- Government Investigation: The DOJ, often with the relevant U.S. Attorney's Office, reviews the case. The government may request extensions to the seal period for further investigation, including subpoenas or interviews.
- Government Decision on Intervention: The government decides whether to intervene (take over the case) or decline. If it intervenes, it leads the litigation, and the relator assists. If it declines, the relator can proceed alone, but success rates are lower (around 20-30% without intervention versus higher with it). The government can still intervene later or dismiss the case if it deems it meritless.
- Litigation and Resolution: If proceeding, discovery and trial follow. Settlements are common to avoid prolonged litigation. To qualify as a relator using publicly disclosed information, one must be an "original source" (e.g., having independent knowledge), as established in Rockwell International Corp. v. United States (2007).
- Bars to Filing: Certain restrictions apply, such as the "public disclosure bar" (preventing suits based solely on publicly available information unless the relator is the original source) and prohibitions on pro se (self-represented) relators.
- Rewards: If the government intervenes and recovers funds, the relator receives 15-25% of the recovery, plus reasonable attorneys' fees and costs. If proceeding alone, the share rises to 25-30%. These percentages can be adjusted based on the relator's contribution. For example, in major cases, relators have received tens of millions.
- Protections: The FCA prohibits retaliation against whistleblowers, such as firing, demotion, or harassment. Relators can sue for reinstatement, double back pay, and other damages. The 1778 Continental Congress law set an early precedent for such protections. Additional laws like the Whistleblower Protection Act bolster these safeguards.
Case/Defendant | Settlement Amount | Year | Description of Alleged Fraud | Relator's Share (if known) |
---|---|---|---|---|
GlaxoSmithKline | $3 billion | 2012 | Illegal marketing of drugs like Paxil and Wellbutrin for unapproved uses, failure to report safety data, and false claims about efficacy, leading to fraudulent Medicare/Medicaid reimbursements. | Not specified (multiple relators) |
Pfizer | $2.3 billion | 2009 | Off-label promotion of drugs like Bextra, violating FDA approvals and resulting in false claims to federal healthcare programs. | Initiated by a sales rep whistleblower |
Johnson & Johnson | $2.2 billion | 2013 | Promoting Risperdal and other drugs for unapproved uses, plus kickbacks to physicians and pharmacists. | Not specified |
HCA Healthcare | $1.7 billion (total across cases) | 2003 | Submitting false Medicare claims, overcharging, and providing unnecessary treatments; separate $631 million settlement for inflating expenses in cost reports. | Two whistleblowers in expense inflation case |
Tenet Healthcare | $900 million | 2006 | Overcharging Medicare and illegal kickbacks for patient referrals. | Not specified |
TAP Pharmaceutical Products | $875 million | 2001 | Fraudulent pricing and kickbacks to doctors to prescribe drugs, affecting Medicare/Medicaid. | Not specified |
Amgen | $762 million | 2012 | Misbranding cancer drugs and deceptive pricing to healthcare programs. | One whistleblower |
United States ex rel. Marcus v. Hess | $54,000 (recovered, plus penalties) | 1943 | Contractors colluded on inflated bids for public works, defrauding the government during Depression-era projects. | Relator received a share |
United States ex rel. Alderson v. Quorum Health Group | $95.5 million | 2001 | Widespread fraudulent hospital billing practices. | Former employee whistleblower |
United States ex rel. Rigsby v. State Farm | Significant jury verdict (amount not specified in sources) | 2016 | Falsely attributing Hurricane Katrina wind damage to flooding to shift costs to federal insurance. | Former adjusters as relators |
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