Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K123320 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Dimension® Ammonia Flex® reagent cartridge / AMM Dimension: The AMM method is an in vitro diagnost... | 2 | 10/11/2018 | Siemens Healthcare Diagnostics, Inc. |
Dimension Vista® Ammonia Flex® reagent cartridge / AMM Dimension: The AMM method is an in vitro dia... | 2 | 10/11/2018 | Siemens Healthcare Diagnostics, Inc. |
Dimension Ammonia (AMM) assay; (Product Number: DF119/10711991) (Mfr: Siemens Healthcare Diagnostics... | 2 | 05/04/2018 | Siemens Healthcare Diagnostics, Inc. |
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