DePuy ASR Recall Lawsuit Filed by 21 Plaintiffs
By Matt O’Donnell
A new lawsuit filed by 21 Plaintiffs who claim to have suffered injuries from the DePuy ASR hip implant has been filed in Madison County Circuit Court. The Plaintiffs are seeking over $350,000 in damages for DePuy ASR side effects and injuries caused by metal poisoning, including tissue loss, bone loss, liver damage, kidney damage, and neurological injuries. The Plaintiffs allege in the DePuy ASR lawsuit that DePuy Orthopaedics and parent company Johnson & Johnson were aware of the side effects of their hip replacement products but failed to warn the public of the risks. According to the DePuy ASR hip implant lawsuit, the companies were notified as early as 2007 by the Australian National Join Replacement Registry that these devices were linked to high failure rates. A year later, in 2008, Newcastle University Hospital concluded that patients implanted with the metal-on-metal ASR hip replacement system were at an increased risk for high blood levels of cobalt and chromium. By that same year, the FDA had received more than 300 reports of problems associated with the DePuy ASR. Despite all of this information, Johnson & Johnson failed to recall the device until August 2010. By that time, thousands of patients had been implanted with a defective hip implant they did not know was defective. Many of these patients have chosen to sue DePuy and Johnson & Johnson for failing to warn them.
Updated August 15th, 2012
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