(PRWEB) June 12, 2012
The US Drug Watchdog says, "Because of the high failure rate associated with the now recalled DePuy ASR hip implant, we think it is absolutely vital to get every DePuy ASR hip implant recipient identified to the best possible attorneys, out of fear the device will fail prematurely, and or out of fear a possible deadline of August 2012 to have all recalled DePuy ASR hip implant recipients identified. Our biggest worry right now is of the 40,000 US citizens, who received a now recalled DePuy ASR hip implant, only about 3400 have been identified by the Ohio Federal Court, that is handling the litigation. Our number one priority is making certain every recalled DePuy ASR hip implant recipient has been identified by the best possible attorneys, so down the road, their rights are protected, should the hip implant fail prematurely." The US Drug Watchdog is encouraging all DePuy ASR recipients to call them, for an unequaled free service, that is focused on making certain no US consumer, that received a DePuy ASR hip implant, that has now been recalled, gets left holding the bag. 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
The US Drug Watchdog indicates symptoms of the recalled DePuy ASR hip implant failure include:
The US Drug Watchdog is the premier advocate for medical device recipients, and pharmaceutical safety in the United States. The group says, "We think it is vital to get all DePuy ASR recipients identified now, because in our opinion it is a very important way to protect their future." 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
DePuy ASR Case Number Ohio Southern Federal District Court Case Number MDL No. 2197