Stryker Recalls Defective Hips

Joe Saunders

Attorney
(866) 735-1102 Ext 340

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A week after the US FDA issued an 11 page warning letter to Stryker Co. about complaints the firm received from January of 2005 to mid 2007 involving the Trident PSL and Trident Hemispherical Acetabular Cups used in hip replacement surgery, Stryker has voluntarily but temporarily withdrawn the defective hip device from the market. The warning letter came after the FDA performed a six week inspection of its Mahwah, NJ plant. The complaints the company received involved poor fitting hip devices requiring a second hip surgery typically referred to as revision surgery.

For more information on this subject, please refer to the section on Medical Devices and Implants.