Medical Device Recalls
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1 result found
510(K) Number: K880231 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09. | 2 | 05/12/2025 | LeMaitre Vascular, Inc. |
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