Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062838 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VITROS Immunodiagnostic Products Troponin I ES Calibrators | 2 | 08/08/2023 | ORTHO-CLINICAL DIAGNOSTICS |
| VITROS Immunodiagnostic Products Troponin I ES Reagent Pack | 2 | 08/08/2023 | ORTHO-CLINICAL DIAGNOSTICS |
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