The US Drug Watchdog is now including the Stryker Rejuvenate, the Biomet M2a Magnum, Wright, and Zimmer Durom Cup, metal on metal hip implant devices to their ongoing initiative involving the DePuy ASR, and DePuy Pinnacle all metal hip implants.
(PRWEB) November 13, 2012
The US Drug Watchdog is now including the Stryker Rejuvenate, the Biomet M2a Magnum, Zimmer Durom Cup, and Wright Medical metal on metal hip implant devices to their ongoing initiative involving the DePuy ASR, and DePuy Pinnacle all metal hip implants. The goal is to identify as many failure victims as possible before the time to get them identified runs out. According to the New York Times on December 27th 2011, "The so-called metal-on-metal hips, in which a device's ball and joint are made of metal, are failing at high rates within a few years instead of lasting 15 years or more, as artificial joints normally do." The US Drug Watchdog wants to hear from any metal-on metal hip implant recipient if their hip implant has already failed, or if the hip implant recipient is suffering the symptoms of a metal-on metal hip implant failure, and the group will provide a metal on metal hip implant recipient with the names, and contacts of who they consider to be the best national caliber attorneys to help them. Recipients of any of the listed metal on metal hip implant devices are encouraged to contact the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via the web site at http://USDrugWatchdog.com.
According to the US Drug Watchdog, "Symptoms of a metal-on-metal hip implant failure include pain in the area of the hip implant, loss of flexibility, swelling in the area of the metal-on metal hip implant, loss of mobility, and elevated levels of cobalt, or chromium in the blood stream of the recipient. We think a blood test for cobalt, and or chromium are the best ways for any metal on metal hip implant recipient, has a failed hip implant device." http://USDrugWatchdog.com
Metal on metal hip implant devices that are now subject to national litigation over failure issues:
DePuy Pinnacle Case Number U.S. District Court for the Northern District of Texas MDL#2244
DePuy ASR Case Number Ohio Southern Federal District Court Case Number MDL # 2197
Stryker Rejuvenate Hip Implant Stem Failure Teleseminar: Metallosis with No Metal on Metal Articulation will address the issues surrounding the latest hip replacement systems recall. On July 6, 2012 Stryker issued a voluntary recall of its Rejuvenate and ABG II modular-neck stems in the United States
Biomet M2a Magnum Metal-on-Metal Hip Replacement U.S. District Court for the Northern District of California. (Case No. 3:12-cv-3476) filed on July 2nd 2012
In re Zimmer Durom Cup Product Liability mass tort litigation, MDL NO. 2158 (SDW), which is pending in the federal District Court in New Jersey (time frame 2006-July 2008)
Wright Medical Technology, Inc., Conserve Hip Implant Products Liability Litigation ("MDL No. 2329"). This is now pending in the U.S. District Court for the Northern District of Georgia
The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device or recalled drug initiative work is the average US consumer never hears about a drug recall or failures involving medical devices like metal-on-metal hip implants. If you have a friend, or loved one who is a recipient of a metal-on metal hip implant that has already failed or is showing symptoms of a failure, or are concerned about a premature failure please call us anytime at 866-714-6466. We want to make certain these metal-on-metal hip implant victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal." http://USDrugWatchdog.com