Medical Device Recalls
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1 result found
510(K) Number: K151628 |
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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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| ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC | 2 | 03/27/2026 |
FEI # 1417592 Medline Industries, LP |
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