Medical Device Recalls
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1 result found
510(K) Number: K934738 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU, Item Number: 170056; ENDO STITCH POLYS... | 2 | 06/14/2017 | Medtronic |
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