Medical Device Recalls
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1 result found
Recall Number: Z-1579-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021/A, H965103028021/EU, H965103028031/A, H... | 1 | 03/26/2026 |
FEI # 1721504 Merit Medical Systems, Inc. |
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