Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K023063 |
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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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| COMP 12MM HUM FRAC STEM MACRO, model # 11-113562 | 2 | 12/29/2017 |
FEI # 1825034 Zimmer Biomet, Inc. |
| Comprehensive Reverse Humeral Fracture Inserter REF 406993 Comprehensive Instrumentation Reverse ... | 2 | 09/30/2011 |
FEI # 1825034 Biomet, Inc. |
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