On August 29, 2016, Stryker Corporation issued an urgent medical device recall related to its Stryker LFIT Anatomic CoCr V40 series of femoral heads due to “higher than expected complaints of taper lock failure.” These femoral heads are used in a number of the company’s modular hip replacement systems (used in hip replacement procedures) such...
RECALLED STRYKER FEMORAL HEAD HIP IMPLANT DANGERS AND LITIGATION UPDATE
