Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K001266 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2 | 2 | 08/12/2024 |
FEI # 1000136573 Ortho-Clinical Diagnostics, Inc. |
| VITROS Immunodiagnostic Products - Folate Reagent Pack(10758750009237) 1513266 | 2 | 10/03/2018 |
FEI # 2250051 Ortho Clinical Diagnostics Inc |
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