Medical Device Recalls
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1 result found
Recall Number: Z-2663-2026 |
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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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| CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidlin... | 2 | 07/02/2026 |
FEI # 3006260740 Bard Access Systems, Inc. |
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