Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K183183 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PDS II (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use... | 2 | 06/14/2024 | Ethicon, Inc. |
| Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product Number J358H | 2 | 11/07/2024 | Ethicon, Inc. |
| PDS®PLUS®VIO®30IN(75CM)®USP6-0(M0.7)®D/A®C-1®MP | 2 | 04/03/2025 | Ethicon Endo Surgery, LLC |
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