FDA Recalls more than 40,000 Stryker LFIT Anatomic V40 Femoral Heads, Patients at Risk of Severe Injuries and Painful Replacement Surgeries
01/06/2017
« Back to News Room FDA Recalls more than 40,000 Stryker LFIT Anatomic V40 Femoral Heads, Patients at Risk of Severe Injuries and Painful Replacement Surgeries In what may be one of the largest hip replacement device recalls in the last decade, The Food and Drug Administration has officially recalled the Stryker LFIT Anatomic V40 Femoral Head. The device is used during total hip re...
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