Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K032367 |
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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| Fem IM Nail 14mmdx48cm left, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee... | 2 | 03/20/2017 |
FEI # 1000220733 Zimmer Biomet, Inc. |
| ASIA ONE-PIECE LAG SCREW | 2 | 02/20/2014 |
FEI # 1000220733 Zimmer, Inc. |
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