Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K213464 |
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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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| HemosIL LMW Heparin Controls; Part Number: 0020300200; | 2 | 08/13/2025 |
FEI # 1217183 Instrumentation Laboratory |
| HemosIL Heparin Calibrators; Part Number: 0020300600; in vitro diagnostic | 2 | 01/24/2025 |
FEI # 1217183 Instrumentation Laboratory |
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