Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K934738 |
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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 |
FEI # 1219930 Medtronic |
| Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071; | 2 | 06/01/2026 |
FEI # 1219930 Covidien, LP |
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