Medical Device Recalls
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1 result found
Recall Number: Z-1915-2026 |
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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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| Pressure Injectable Arrowg+ard Blue Plus® Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)1080... | 2 | 04/22/2026 |
FEI # 3013162291 ARROW INTERNATIONAL, LLC |
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