Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K962819 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dimension Gentamicin Flex reagent cartridge, DM GENT, gentamicin enzyme immunoassay, Lot numbers af... | 2 | 06/13/2018 | Siemens Healthcare Diagnostics, Inc. |
| Dimension Vista Gentamicin Flex reagent cartridge, DV GENT, gentamicin enzyme immunoassay. Affected... | 2 | 06/13/2018 | Siemens Healthcare Diagnostics, Inc. |
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