Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K960749 |
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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. |
| Hemochron Jr. ACT- LR Assay (JACT- LR); ITC Catalogue/Code Number: JACTLR 45 Cuvettes; For Perfor... | 2 | 08/21/2009 |
FEI # 1000526865 International Technidyne Corp. |
| Hemochron Jr. Whole Blood Microcoagulation system Low Range Activated Clotting Time. ACT-LR Cuvette... | 3 | 08/23/2005 |
FEI # 1000526865 International Technidyne Corp. |
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