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US Drug Watchdog Now Urges All Metal Hip Implant Recipients to Get a Blood Test for Elevated Metals Levels Out of Fear of Side Effects Related to Cobalt or Chromium
Date:1/29/2013

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
  • 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 a blood test to see if their device has already failed, and if the worst has happened we want to help them get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal." http://USDrugWatchdog.com

    Read the full story at http://www.prweb.com/releases/2013/1/prweb10350721.htm.


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