Medical Device Recalls
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1 result found
Recall Number: Z-2894-2026 |
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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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| 5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905 | 2 | 08/05/2026 |
FEI # 3005017664 Aniara Diagnostica LLC |
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