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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K931847
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Product Description
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Recall
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FDA Recall
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Stryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-, Allows the user to mix bon... 2 09/19/2023 FEI # 3015967359
Stryker Corporation
Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle & Prox. Med. Press-... 2 09/19/2023 FEI # 3015967359
Stryker Corporation
Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle & Solid Blades-Allo... 2 09/19/2023 FEI # 3015967359
Stryker Corporation
Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle-Allows the user to ... 2 09/19/2023 FEI # 3015967359
Stryker Corporation
Stryker ACM (Advanced Cement Mixing): 180-Gram Cement Cartridge with Breakaway Femoral Nozzle-Allows... 2 09/19/2023 FEI # 3015967359
Stryker Corporation
Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway Nozzle, Restrictors & Prox.... 2 09/19/2023 FEI # 3015967359
Stryker Corporation
Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway Nozzle, Restrictors & Prox.... 2 09/19/2023 FEI # 3015967359
Stryker Corporation
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