Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060264 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dimension IRON Flex reagent cartridges | 3 | 11/11/2016 |
FEI # 2517506 Siemens Healthcare Diagnostics, Inc. |
| Dimension Vista IRON Flex reagent cartridges | 3 | 11/11/2016 |
FEI # 2517506 Siemens Healthcare Diagnostics, Inc. |
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