Medical Device Recalls
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1 result found
Recall Number: Z-0880-2026 |
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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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| Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron... | 2 | 12/03/2025 |
FEI # 2250033 Accriva Diagnostics, Inc. |
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