Because Of Possible Deadline US Drug Watchdog Calls Its Identification of All ASR DePuy Hip Implant Recipients Its Most important Medical Device Initiative of 2012

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The US Drug Watchdog says, "Our ASR DePuy recalled hip implant initiative is our most important recalled medical device initiative at this moment because we might have a deadline of August 2012 to get all recalled DePuy ASR hip implant recipients to the federal court in Ohio. At this point we do not care if the recalled DePuy ASR metal on metal hip implant has failed yet or not, we want to get these hip implant recipients to the best possible attorneys." Most worrisome to the US Drug Watchdog is the fact that the DePuy ASR hip implant was sold as the right hip implant for younger adults who wanted to have an active or athletic lifestyle. The group talks to DePuy ASR recipients almost every day, who are now crippled, or living in enormous pain, and they are offering to help all DePuy ASR recipients get identified to the best possible attorneys. For more information about the DePuy ASR hip implant recall please call the US Drug Watchdog at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

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At this point we do not care if the recalled DePuy ASR metal on metal hip implant has failed yet or not, we want to get these hip implant recipients to the best possible attorneys

The US Drug Watchdog is calling its initiative to identify all recipients of the recalled DePuy ASR hip implant, its most important recalled medical device initiative of 2012, because of a possible looming deadline of August 2012. The group says, "ASR DePuy hip implants are failing, or have failed at an unacceptably high rate. As a result there was a recall on this hip implant device in August of 2010. DePuy ASR hip implants were surgically implanted on tens of thousands of US citizens between 2005 and early 2010." According to the US FDA, symptoms of a recalled ASR DePuy hip implant failure include pain in the hip region, problems walking, swelling of the hip, lack of flexibility in the area of the hip, and elevated levels of cobalt in the recipients blood stream. The US Drug Watchdog is urging family members of hip implant recipients, who received a hip implant between 2005, and mid 2010, to ask if the hip implant was a DePuy ASR? The US Drug Watchdog says, "If you, or a loved one has had a hip replacement involving the recalled ASR DePuy hip implant, please call us immediately at 866-714-6466, and we will do everything possible to get you meaningful help from the best possible attorneys." http://USDrugWatchdog.com

The US Drug Watchdog is the premier private recalled pharmaceutical, and medical device watchdog in the United States. The group says, "We want to make certain all DePuy ASR hip implant victims get to the actual trial law firms or attorneys that have the best record in achieving superior results for their clients--period--not a middleman marketing law firm, or cable TV attorney." For more information please contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via its web site at http://USDrugWatchdog.com

Ohio Southern Federal District Court Case Number MDL No. 2197

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M Thomas Martin
Americas Watchdog
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