Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K093844 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles; Part Number: 72201805 Bi... | 2 | 09/17/2013 | Smith & Nephew, Inc. Endoscopy Division |
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