DePuy ASR Hip Implant Lawsuit Filed By Ohio Woman
By Mike Holter
An Ohio woman who needed revision surgery only two years after being implanted with a DePuy ASR hip implant has decided to sue DePuy Orthopaedics, a division of Johnson & Johnson, for selling a defective device and for failing to warn the public about its side effects. The DePuy ASR has come under fire recently following a massive August 2010 recall that first alerted the public that these all-metal hip replacement systems are linked to a host of serious complications, including the necessity to undergo risky revision surgery.The unnamed Ohio Plaintiff alleges in the DePuy ASR lawsuit, filed August 8, 2012 in the DePuy ASR MDL, that she suffered serious side effects from the metal-on-metal hip implant, including elevated levels of cobalt and chromium in her blood. This caused her to suffer kidney failure, chronic pain and suffering, infection, painful rehabilitation, hip aspiration, extended hospitalization, and overall loss of quality of life, her DePuy ASR lawyer says. The Plaintiff was implanted with the DePuy ASR hip replacement system in her right hip in January 2007, and had to remove the implant on November 18, 2008. Her lawsuit alleges she was not aware that her injuries were caused by the DePuy ASR until she became aware of the recall. She is suing DePuy for failure to warn her and the public of the risk of metal-on-metal hip implant side effects as soon as the company became aware of them.
Updated August 21st, 2012
{loadposition content_postads}
All medical device, dangerous drug and medical class action and lawsuit news updates are listed in the Drug and Medical Device section of Top Class Actions.
Top Class Actions Legal Statement

