Stryker Ceramic Hip Recall

Stryker recalled its rejuvenate abg ii and accolade modular neck hip stems after the implants showed signs of corroding and fretting. Stryker lfit anatomic v40 femoral head class 2 device recall august 29 2016. In february 2001 the fda announced that biomet us manufacturer of artificial hips had made a voluntary recall of its hip replacement system following discovery of defects in the zirconia ceramic.

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