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All product recalls associated with Stryker Instruments Div. of Stryker Corporation.
Total Recalls
148
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2022
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.
Mis-labeling; The instructions for use include a use for which the device is not intended. (Device not approved to capture a bone biopsy)
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)