Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K093441 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dimension Vista Digoxin (DIGXN) Flex reagent cartridge | 2 | 05/05/2017 | Siemens Healthcare Diagnostics, Inc. |
| Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnos... | 2 | 04/18/2013 | Siemens Healthcare Diagnostics, Inc. |
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