Biomet Hip Replacement Device Recalled by FDA
The Law Firm of Lytal, Reiter, Smith, Ivey & Fronrath wants you to know that a report released Tuesday, November 27, 2018 on NBC’s Today Show indicates that the hip replacement device produced by Biomet has been recalled by the FDA. But this comes years after research showed that the device could become harmful and possibly cause death in the patient a short time after surgery. “By 2015, regulators in Australia, Germany, and five other countries were already issuing warnings about the product. But in the U.S., the Food and Drug Administration, which oversees medical devices, was silent.” The Olympic gold medal gymnast , Mary Lou Retton had the surgery and even became a spokesperson for the device but today suffers from the very same serious problems that many others are now facing. Our law firm has been helping victims of medical malpractice for over thirty years. We have a department dedicated to specifically addressing this very issue.
If you or a loved one has had a hip replacement where the Biomet M2a device was used or another manufacturers device and are suffering from pain or other related issues caused by the device after surgery, we want you to call the West Palm Beach law office of Lytal, Reiter, Smith, Ivey & Fronrath at 561-655-1990 or inquire at www.ForYourRights.com
