Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K073055 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dimension Enzymatic Creatinine Flex reagent cartridge, DF270. The ECRE method is an in vitro d... | 2 | 12/13/2008 | Dade Behring, Inc. |
| Siemens Dimension(R) EZCR Flex(R) Reagent Cartridge. Catalog number DF270B. In vitro diagnostic te... | 2 | 05/10/2011 | Siemens Healthcare Diagnostics, Inc. |
| Dimension Assays: ENZYMATIC CREATININE | 2 | 05/11/2016 | Siemens Healthcare Diagnostics, Inc. |
| Dimension Enzymatic Creatinine (EZCR) reagent, SMN 10471520 | 2 | 01/24/2020 | Siemens Healthcare Diagnostics, Inc. |
| Dimension Enzymatic Creatinine, Siemens Material Number 10471520, UDI Number 00842768030512 - Produc... | 2 | 06/05/2020 | Siemens Healthcare Diagnostics, Inc. |
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