Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K190807 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VITROS XT Chemistry Products TBIL-ALKP Slides | 2 | 09/21/2023 |
FEI # 1000305840 Ortho-Clinical Diagnostics, INc. |
| VITROS XT Chemistry Products TBIL-ALKP Slides (ALKP is not affected) In Vitro Diagnostic use only - ... | 2 | 08/24/2020 |
FEI # 1000305840 Ortho-Clinical Diagnostics |
| ORTHO CLINICAL DIAGNOSTICS INC TOTAL BILI-ALKP XT (L-SEQUESTER) (300/PK) REAGENT. | 2 | 05/27/2025 |
FEI # 3004386693 Mckesson Medical-Surgical Inc. Corporate Office |
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