MDL Sought For Stryker LFIT V40 Femoral Head Following Failures, Recall

Mealey's (January 31, 2017, 12:32 PM EST) -- WASHINGTON, D.C. — A plaintiff on Jan. 13 asked the Judicial Panel on Multidistrict Litigation to centralize six cases involving the now-recalled Stryker LFIT V40 CoCr Anatomic Femoral head orthopedic device in an MDL in the U.S. District Court for the District of Massachusetts (In Re:  Stryker Orthopaedics LFIT V40 Femoral Head Product Liability Litigation, MDL Docket No. 2768)....

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