Medical Device Recalls
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1 result found
Recall Number: Z-1174-2017 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments f... | 2 | 02/22/2017 |
FEI # 3002806535 Biomet U.K., Ltd. |
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