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US Drug Watchdog Now Offers all Metal Hip Implant Recipients Concerned About a Premature Device Failure the Names of the Best Law Firms-Don’t Get Left Holding the Bag

September 12, 2012

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 concerned about a premature failure of a metal-on metal hip implant, 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. The US Drug Watchdog is calling the US metal on metal hip implant disaster the biggest medical device failure in US history, and they are convinced there are hundreds of thousands of US citizens who are recipients of a metal-on-metal hip implant that has failed, or will fail prematurely. 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.” Recipients of a metal on metal hip implant 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

(PRWEB) September 11, 2012

The US Drug Watchdog is now calling their defective, or failed metal-on-metal hip implant compensation, and representation initiative their largest medical device victims campaign ever. The goals of this campaign is compensation for what a victim of a metal-on-metal hip implant failure will have to go through, and making certain every victim of a metal-on-metal hip implant has the best possible attorneys, or law firms. The US Drug Watchdog says, “There are 500,000 US citizens with metal on metal hip implants, and we fear a failure rate of 50%. 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 will not stand by as hundreds of thousands of US citizens get left on the curb holding the bag for a problem that should not be their’s.” All US metal on metal hip implant recipients are encouraged to call the US Drug Watchdog anytime at 866-714-6466 for more information, or they can contact the group via their 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

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 insure 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/prweb2012/9/prweb9876928.htm


Source: prweb



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