Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K103002 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 REF 04.019.028S Manufactured... | 2 | 07/23/2012 |
FEI # 3005180112 Synthes USA HQ, Inc. |
| 4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 REF 04.019.038S Manufactured... | 2 | 07/23/2012 |
FEI # 3005180112 Synthes USA HQ, Inc. |
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