Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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Z-1017-2010 - Dimension Vista System BUN Flex Reagent Cartridge, Catalog number K1021, in vitro diagnostic. | 2 | 03/08/2010 | Siemens Healthcare Diagnostics, Inc. |
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