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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-1141-2017 - Dimension Vista® Ammonia Flex® reagent cartridge / AMM Dimension: The AMM method is an in vitro diagnostic test for the quantitative measurement of ammonia in human plasma on the Dimension clinical c... 2 10/11/2018 FEI # 2517506
Siemens Healthcare Diagnostics, Inc.
Z-1140-2017 - Dimension® Ammonia Flex® reagent cartridge / AMM Dimension: The AMM method is an in vitro diagnostic test for the quantitative measurement of ammonia in human plasma on the Dimension clinical chemis... 2 10/11/2018 FEI # 2517506
Siemens Healthcare Diagnostics, Inc.
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