Medical Device Recalls
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21 to 22 of 22 Results
PMA Number: P010014 |
Results per Page |
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 Right Medial Size C Product Usage: Instruments ... | 2 | 02/22/2017 | Biomet U.K., Ltd. |
Oxford Femoral Knee System REF 154600, LOT 2272736, WARNING DO NOT RESTERILIZE, STERILE UNLESS PACK ... | 2 | 06/29/2011 | Biomet U.K., Ltd. |
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