Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K042476 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic use only. CATALOG #(s): 68017... | 2 | 02/19/2019 |
FEI # 1000305841 Ortho-Clinical Diagnostics |
| VITROS¿ Valproic Acid (VALP) Reagent, REF/Catalog No. 6801710 --- Ortho- Clinical Diagnostics Roche... | 2 | 02/08/2012 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
| VITROS VALP Reagent , REF 680 1710. Each box contains 6 packs. Each pack contains liquid reagent f... | 2 | 06/04/2005 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
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