Stryker Ceramic Hip Recall

After receiving an fda warning letter the company stated that its trident psl and hemispherical acetabular cups were safe and reliable but it voluntarily recalled the products because they did not meet company standards in residual tests. Stryker lfit anatomic v40 femoral head class 2 device recall august 29 2016. Shortly after the announcement and warning stryker initiated a voluntary recall of its two problem hips.

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