Medical Device Recalls
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1 result found
510(K) Number: K071224 |
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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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Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12 Flex Reagent Cartridg... | 2 | 06/27/2012 | Siemens Healthcare Diagnostics, Inc. |
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