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All product recalls associated with Stryker Instruments Div. of Stryker Corporation.
Total Recalls
264
Past Year
21
Class I (Serious)
0
Most Recent
Oct 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Instructions have been updated to include new warnings regarding percutaneous pin placement during surgery in order to mitigate the risk of femur fractures.
Mis-labeing; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)
Mis-labeling; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)