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Stryker Recall Litigation in New Jersey Now Includes More than 2,000 Lawsuits over Rejuvenate, ABG II Metal Hips, Bernstein Liebhard LLP Reports
Date:7/18/2014

ilarly accuse Stryker Orthopaedics of failing to adequately warn about metal hip side effects prior to a U.S. Food and Drug Administration (FDA) recall on July 6, 2012 that was prompted by company knowledge that the devices may fret and corrode at the modular-neck junction. In turn, patients may experience swelling, pain and other adverse tissue reactions, Stryker said in its recall announcement. Following the recall, the company advised on its website that all Rejuvenate and ABG II hip recipients to undergo routine medical testing and cross-sectional imaging to monitor for early device failure complications.*

Stryker lawsuits are also moving forward in the U.S. District Court, District of Minnesota, where a federal multidistrict litigation (MDL) now includes hundreds of cases. A Case List updated on July 15th shows 1,692 similar actions over the Rejuvenate and ABG II implants. Not unlike metal hip claims filed in New Jersey, plaintiffs in these cases similarly allege chronic pain, osteolysis, tissue necrosis, metallosis and other complications stemming from the devices. (In re: Stryker Rejuvenate and ABG II Hip Implant Products Liability Litigation, No. 244)

Individuals who were allegedly harmed by the Rejuvenate and ABG II hip stems may be eligible to file their own Stryker hip lawsuit. Learn more about lawsuits filed in the wake of 2012’s Stryker hip recall when you visit Bernstein Liebhard LLP’s website, or call 800-511-5092 to arrange for a free, no-obligation case review
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