US Drug Watchdog Will Now Help All Recipients of the Recalled DePuy ASR Hip Implant Get to the Best Possible Attorneys Even if the Hip Implant Has Not Yet Failed

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The US Drug Watchdog says, "We want to hear from every recipient of a DePuy ASR hip implant, out of fear their device has not yet failed, or it has started to fail, and the individual may not know the warning signs of a failure. Symptoms of a DePuy ASR hip implant failure include pain, problems walking, swelling of the hip, or lack of flexibility." There are close to 40,000 US citizens, who received a DePuy ASR hip implant between 2005, and 2010, and the US Drug Watchdog wants to hear from every recipient, in order to see if their DePuy ASR hip implant has failed, or is in the process of failing. The group says, "It has already been well documented that there is an extremely high failure rate for the DePuy ASR hip implants. We have heard from hundreds of DePuy ASR hip implant recipients, and we now believe its vital to get every victim, or potential victim identified as soon as possible, in order to try to assist them in getting meaningful help, and the best possible attorneys." They say, "If you, or a loved one has had a hip replacement involving the recalled DePuy ASR hip implant, be please call us immediately at 866-714-6466." http://USDrugWatchdog.Com

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We urgently need family members, or loved ones of a hip implant recipient, that was surgically installed between 2005, and early 2010 to ask the family member, or friend, if it was a DePuy ASR hip implant.

The US Drug Watchdog says, "We are offering to assist every recipient of a DePuy ASR hip implant to determine if their hip implant has already failed, it is in the process of failing, or explain what we know about the potential for failures. We urgently need family members, or loved ones of a hip implant recipient, that was surgically installed between 2005, and early 2010 to ask the family member, or friend, if it was a DePuy ASR hip implant." They say, "Many US DePuy ASR hip implant victims are elderly, or senior citizens, and we are very worried the majority of victims will not complain, even if they are suffering pain, having problems walking, have swelling of the hip, or have lost flexibility. These hip implants were also sold to younger adults as the quote en quote athletic hip implant, for adults wanting an active lifestyle." They say, "According to numerous studies the DePuy ASR hip implant has a very high failure rate, and we think its vital, we do our best to identify all victims." The US Drug Watchdog fears there are 10,000's US DePuy ASR hip implant recipients living in horrible pain, or they are not aware of the recall. The group says, "We could easily have tens of thousands of US DePuy ASR hip implant victims, living each day with a failed hip implant. Nothing is more important to us than trying to getting all DePuy ASR hip implant victims identified, and we will help with the process." 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.

Important Update: The US Drug Watchdog says, "According to a published report in the New York Times on December 27th 2011, only 3300 individuals, who have received a DePuy ASR hip implant have been identified by the Federal District Court in Ohio. We think the number of identified recipients, or victims should be closer to 15,000 to 20,000 already identified, so we intend to dramatically ramp up our efforts to get all DePuy ASR hip implant recipients identified."

The US Drug Watchdog's ASR DePuy hip implant failure symptoms include:

  • Pain in the Hip Region
  • Problems While Walking or The Inability to Walk
  • Swelling of the Hip
  • General Discomfort
  • Lack of Flexibility

The US Drug Watchdog is the premier medical device and pharmaceutical watchdog in the United States. The group says, "We want to make certain all Depuy ASR hip implant victims get to top notch national caliber trial law firms, or attorneys, that have the best record in achieving superior results for their clients with recalled, or defective medical devices." 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 Federal District Court Federal Case Number MDL No. 2197

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M Thomas Martin
Americas Watchdog
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