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DrugRisk Adds Update on Stryker Hip Recall: Claims Could Cost $190 to 390 Million
Date:3/29/2013

Chicago, IL (PRWEB) March 29, 2013

The hip implant resource center at DrugRisk.com is announcing new information on the site for patients that may have been affected by the recent Stryker hip recall. The company has informed investors they are attempting to resolve claims as patients alleging injury have requested cases be moved to a federal court.

DrugRisk was created to provide patients using popular drugs and medical devices with the latest warnings, recalls, studies and litigation news. Visitors can learn if others are experiencing similar side effects and decide if they need legal advice.

The resource center contains warnings from the British Medical Journal* and FDA** that toxic metal shavings from all-metal hips like the Stryker ABG II and Rejuvenate can cause serious conditions such as tissue damage, bone loss and damage to other organs when released into the body.

Stryker issued a recall of the Rejuvenate and ABG II modular implant systems in July of 2012***. As part of the recall, the company admitted some patients experienced adverse local tissue reactions or elevated levels of metal in the bloodstream, even if no symptoms were present***.

So far, more than 80 patients affected by the hip recall have filed Stryker lawsuits in a New Jersey multi-district court****.

DrugRisk has also learned that patients filed a petition with the U.S. Judicial Panel on Multidistrict Litigation asking that Stryker lawsuits be consolidated to a special federal court in the U.S. District Court, District of Minnesota. (In Re: Stryker Rejuvenate and ABG II Hip Implant Products Liability Litigation, Case Pending No. 20 (JPML))

Now, Stryker has advised investors that costs assoc
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