Olympus Settles Largest Kickback Lawsuit for a Medical Device Company in U.S. History


Still reeling from the contaminated medical scopes scandal, Olympus Corp. (Tokyo) is making headlines for another unseemly bit of business. Its U.S. subsidiary, Olympus Corp. of the Americas (Center Valley, PA), has agreed to pay $623 million to resolve a civil whistleblower lawsuit and criminal charges for violating the U.S. Anti-Kickback Statute (AKS). The settlement is the largest total amount paid in U.S. history for violations of the AKS and the largest amount ever paid by a medical device company, according to Kenney & McCafferty, P.C., the law firm representing the whistleblower.

The court filings, which were unsealed yesterday, revealed a rampant “corporate culture of fraud and herd mentality,” said Kenney & McCafferty. The medical device company engaged in an “elaborate international kick-back scheme” to sell its medical equipment, using tactics such as:

  • providing key accounts with “permanent loans” of Olympus medical equipment virtually whenever requested by Olympus sales and marketing personnel to maintain customer loyalty to the Olympus brand and to secure purchases of Olympus products;
  • funneling cash payments of as much as $100,000 annually  to reward “VIP” physicians for ostensible “consulting services”  at the discretion of Olympus sales and marketing representatives, with the knowledge and endorsement of senior management, based on sales potential;
  • making annual cash payments of hundreds of thousands of dollars masquerading as “grants” to fund educational or research programs made at the discretion of a grant committee comprised solely of Olympus sales and marketing personnel, based on sales potential; and
  • funding luxury, all-expense paid vacations to Japan and other exotic international destinations for “VIP physicians,” and sometimes their spouses, in exchange for purchases and promotion of Olympus medical products. […]

“Olympus is not unique in putting profits before people’s lives,” says Diana Zuckerman, PhD, president of the National Center for Health Research (Washington, D.C.), as reported by sister brand Qmed. “But, we can hope that when companies get caught and fined, that has a chilling effect on other companies that are behaving similarly or considering doing so.” […]

Earlier this year, Olympus and FDA came under U.S. Senate scrutiny for the company’s duodenoscopes, a type of endoscope used in certain medical procedures, which are difficult to clean and, as a result, sickened hundreds of patients in the United States and Europe. The contaminated scopes were linked to more than two dozen outbreaks of antibiotic-resistant infections and are associated with the deaths of more than a dozen people. Olympus initially denied that the design of the scope was connected to these outbreaks and blamed improper cleaning procedures at the hospitals. The Senate health committee report also places responsibility on regulatory oversight, noting that “FDA’s current system to monitor medical device safety is unable to effectively identify device problems when they occur.” For more on this, read “Lax FDA oversight allowed dirty medical scopes scandal to spread, says Senate report.”

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