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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K943323
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Product Description
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Recall
Class
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FDA Recall
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Stryker Cordless Driver 3 Handpiece. Stryker Instruments, Kalamazoo, MI; REF 4300. The devic... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Rotary Handpiece, Single Trigger, For use with Stryker System 6. Stryker Instruments, Kalam... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Rotary Handpiece, Single Trigger, For use with Stryker System 6. Stryker Instruments, Kalam... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Rotary Handpiece, Dual Trigger, For use with Stryker System 6. Stryker Instruments, Kalamaz... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Precision Oscillating Tip Saw, For use with Stryker System 6. Stryker Instruments, Kalamazo... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Reciprocating Saw, For use with Stryker System 6. Stryker Instruments, Kalamazoo, MI; REF 62... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Sternum Saw, For use with Stryker System 6. Stryker Instruments, Kalamazoo, MI; REF 6207. ... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Sagittal Saw, For use with Stryker System 6. Stryker Instruments, Kalamazoo, MI; REF 6208. ... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Sagittal Saw, For use with Stryker System 6. Stryker Instruments, Kalamazoo, MI; REF 6208-0... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
Stryker Rotary Handpiece, Dual Trigger, For use with Stryker System 6. Stryker Instruments, Kalamaz... 2 03/10/2009 Stryker Instruments Div. of Stryker Corporation
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