Medical Device Recalls
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1 result found
510(K) Number: K031286 |
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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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| Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture | 2 | 10/26/2016 |
FEI # 2916714 Aesculap Implant Systems LLC |
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