In january 2008 stryker issued a recall for two products from their trident hip implant line the trident acetabular psl cup and the trident hemispherical cup after it was discovered that. According to the fda medical device recall database the company received multiple complaints from patients who were injured after the taper lock on the femur head failed. Stryker also recalled hip implants in 2008 because of manufacturing issues.
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