Biomet Hip Replacements
In September 2001, the Food and Drug Administration (FDA) informed the public that Biomet, and seven other firms that manufacture medical devices in the United States, conducted a recall of their hip implants. This product withdrawal from the market was caused by the problems found on a component of the hip implant that could fracture, resulting in the need for another surgical replacement. The component that was found defective was the femoral head of the hip implant that was made of zirconia ceramic. This is the ball portion of the synthetic hips that are used in surgeries for hip replacements.
St. Gobain Desmarquest of France was the distributor of this defective femoral head. This femoral head was contained in all products for Biomet hip replacements and seven other manufacturers of medical products, including DePuy Orthopedics Inc., Zimmer Inc., Smith & Nephew Inc., Apex Surgical LLC, Osteoimplant Technology Inc., Stryker Howmedica Osteonics and Encore Orthopedics Inc. The recall was issued for all the hip implants with defective components from all manufacturers and applies to those that were made after January of 1998.
A recipient of a hip implant would know that the structure was fractured when he or she displays symptoms that include a grinding sensation at the hip, hip pain, or limited range of motion. An audible popping noise sometimes occurrs before the fracturing of the femoral head. The synthetic hips that are at risk for these fractures tend to break 19 to 28 months after they are surgically implanted. An estimated six percent of the 150,000 to 200,000 patients that undergo surgeries for hip replacements every year receive a synthetic hip that contains this defect.
It is possible that you were a recipient of a defective medical device if you underwent a surgery that used a Biomet hip replacement. If this is so, and you are currently suffering from symptoms, contact a lawyer. A lawyer who is experienced in defective medical device claims can give you the answers that you are looking for. With experienced firms, it is expected that consultation services are provided free of charge. At this meeting, your attorney can assess your medical records and see that you receive the compensation you deserve for your ailments.
If you are looking for retributions for Biomet hip replacement injuries, here are some useful tips to consider:
Research prospective attorneys before selecting one to represent you. An ideal attorney should have years of experience managing defective product or personal injury claims. While this might take some time and dedication, your hard work will pay off when you are finally able to locate the best attorney to meet your needs. Review caseloads, previous experience, and the reputations of attorneys in your area, and set up consultation meetings so that your claim can be reviewed. Free of charge, these meetings can provide you with the resources needed to initiate the lawsuit.
Keep track of all medical records, expenses, employment disability paperwork, and doctor visits, as all of these may provide your attorney with evidence needed to win your case.
Work with your attorney and the defendant to reach a fair settlement. The purpose of the lawsuit is to have the defective product recalled and receive compensation for expenses, not to inaccurately accuse individuals of negligence. While you want to be compensated for your losses, claims should also be within reason.
If your hospital still held you responsible for co-pays or for prescription medications costs, you may be eligible for reimbursements. A hospital should never benefit financially from medical device malfunctioning.
Act quickly. There is not limitless time available to make these claims. Contact an attorney, and set up a meeting right away.
