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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K063206
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FDA Recall
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Dimension Vista® Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in v... 2 07/19/2016 CSL Behring GmbH
Siemens Dimension Vista Homocysteine Flex Reagent Cartridge The HCYS method is an in vitro diagno... 2 12/19/2013 Siemens Healthcare Diagnostics, Inc.
Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an in vitro diagnostic ... 3 11/06/2012 Siemens Healthcare Diagnostics, Inc.