Medical Device Recalls
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1 result found
510(K) Number: K100344 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measu... | 2 | 08/29/2022 | Siemens Healthcare Diagnostics, Inc. |
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