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US Drug Watchdog Now Offers to Provide All US Metal on Metal Hip Implant Recipients the Names of the Best Law Firms–500,000 Potential US Victims

August 16, 2012

The US Drug Watchdog says, “According to the New York Times on December 27th 2011 there are 500,000 US citizens, who are recipients of a metal on metal hip implant. The Europeans are now suggesting failure rates of metal on metal hip implants of 50%, and they may soon be requiring blood testing to determine if a metal on metal hip implant has failed. Our goal is to identify at least 250,000 plus US recipients of metal on metal hip implants to the best possible attorneys, because we do not want completely innocent US metal on metal hip implant recipients left holding the bag for a problem that should not be their’s.” As of this moment under 5,000 US citizens, who have a failed metal on metal hip implant have been identified by federal courts in Ohio, and or Texas handling the DePuy litigation. But DePuy is not the only metal on metal hip implant manufacturer in question. The US Drug Watchdog is now describing their All Metal on Metal Hip Implant Initiative the biggest medical device failure in US history. For more information US metal on metal hip implant recipients are encouraged to call the US Drug Watchdog anytime at 866-714-6466, or they can contact the group via their web site at http://USDrugWatchdog.com

(PRWEB) August 16, 2012

The US Drug Watchdog says, “We want 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, or the metal on metal hip implant recipient is concerned about a premature failure. We are talking about 500,000 US citizens with metal on metal hip implants, with a possible 50% plus failure ratio. We will provide a metal on metal hip implant recipient with the names, and contacts of who we consider to be the best national caliber attorneys to help them.” 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. 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.” Victims of the US Metal on Metal Hip Implant Disaster 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

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, such as swelling, pain in the region of the hip, loss of flexibility, loss of mobility, and most importantly elevated levels of cobalt, and or chromium in a all metal hip implant recipients blood stream, please have them call us at 866-714-6466 immediately. 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

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 No. 2197AAJ

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.

For the original version on PRWeb visit: http://www.prweb.com/releases/prweb2012/8/prweb9757963.htm


Source: prweb



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