Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061719 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dimension Vista® Total Bilirubin Flex® reagent cartridge -In vitro Diagnostic for the determinatio... | 2 | 03/20/2020 | Siemens Healthcare Diagnostics, Inc. |
| Dimension Vista® Total Bilirubin (TBIL) Flex Reagent Cartridge; Siemens Material Number (SMN): 10445... | 2 | 09/06/2024 | Siemens Healthcare Diagnostics, Inc. |
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