Medical Device Recalls
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1 result found
510(K) Number: K043438 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B | 1 | 03/26/2026 |
FEI # 1721504 Merit Medical Systems, Inc. |
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