Stryker Ceramic Hip Recall

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. The devices have been prone to failure at higher than usual rates causing painful side effects such as tissue damage metallosis and implant replacement. Stryker hip implant recall history howmedica osteonics corporation which operates under the name of stryker orthopaedics recalled the stryker rejuvenate modular primary hip system and the stryker abg ii modular neck hip system in the united states back in june 2012.

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