Senator Charles Grassley (R-Iowa) sent a letter to Zimmer Holdings in July, asking the company to provide information about how it handles reports of possible product issues sent by medical consultants. The senator also requested information about how Zimmer Holdings tracks the success and failure of its artificial hips and knees.
According to the 7/30/10 edition of the New York Times, Dr. Lawrence Dorr, who worked as a consultant for Zimmer, raised concerns in 2008 with other orthopedic surgeons that the Zimmer Durom cup was failing a few years after implant. Patients who experienced failure of their device required replacement surgery.
Zimmer, however, responded by blaming Dorr's technique. The company reportedly convinced the US Food and Drug Administration (FDA) to close its investigation by sending data showing that the Zimmer Durom cup worked well.
In June 2010 two of the doctors who provided the FDA with that research told the New York Times that the devices started failing after that data was sent. One of the doctors says the problem was not Dorr's technique but simply that Dorr was implanting the device before other surgeons, the result being that the devices he implanted failing before those implanted by other surgeons.
Zimmer defended its Durom cup as safe.
READ MORE ZIMMER DUROM CUP LEGAL NEWS
Zimmer is not required by law to track the long-term performance of its devices; however, Senator Grassley has requested information on whether the company does any such tracking.
The letter, published on fdanews.com, gives Zimmer until August 12 to respond to Senator Grassley's questions. In his letter, Senator Grassley noted that he was "troubled" by the Times article about Zimmer's response to safety concerns raised by consultants.
A Zimmer spokesperson said the company "welcomed the opportunity" to speak with Senator Grassley.