Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K101921 |
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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 Intact PTH Reagent Pack- IVD For the quantitative measurement of i... | 2 | 01/04/2023 |
FEI # 1000136573 Ortho-Clinical Diagnostics, Inc. |
| VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 68028... | 2 | 12/23/2016 |
FEI # 3007111389 ORTHO-CLINICAL DIAGNOSTICS |
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