Hip Makers Must Report Patient Symptoms to FDA


After a growing number of complaints concerning a metal-on-metal hip implant made by DePuy Orthopaedics, the Food and Drug Administration has required that makers of the hips analyze patient symptoms after surgery. The company Johnson & Johnson has agreed to pay for “reasonable and customary costs of monitoring” of this hips. Around 20 hip manufacturers are required to report patient progress. Metal-on-metal implants have a higher risk factor due to the friction of metal rubbing on each other, releasing metal into the bloodstream, resulting in allergies, tissue damage, and infection. Metal released into the bloodstream could also cause heart and neurological issues.

According to news reports, a scientist from the FDA will conduct follow-up studies to determine the harm metal does in the bloodstream. Blood samples will be collected. An orthopedic surgeon advises that patients be aware of pain, numbness, or swelling that occurs after surgery. Researchers are currently developing sturdier implants that will last as long as 30 years. As a Baltimore car accident lawyer, I hope that anybody experiencing pain after surgery consult with their doctor immediately. If you or a loved one experienced a defective hip implant, discuss your case with a Baltimore personal injury lawyer who can evaluate your claim.