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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 30 Results
510(K) Number: K081543
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VITROS 5600 Integrated System --- For use in the in vitro quantitative, semi-quantitative, and quali... 2 08/01/2014 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Product Code/Catalog Number 6802413 for in vitro diagnostic use. 2 06/09/2014 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System (product code 6802413) Product Usage: For use in the in vitro qua... 2 07/02/2013 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Product Code 6802413. Intended for use in the measurement of a var... 2 04/13/2013 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System Software For use in the in-vitro quantitative, semi quantitative, ... 2 07/23/2012 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System Software Version 1.6 & Below Product Usage: For use in the in vi... 2 06/01/2012 FEI # 1000305841
Ortho-Clinical Diagnostics
VITROS&amp;amp;amp;amp;reg; 5600 Chemistry System, Product Code: 6802413 Product Usage: Fo... 2 04/26/2012 FEI # 1000305841
Ortho-Clinical Diagnostics
VITROS Immunodiagnostic Products - TSH Reagent Pack (10758750000227) 1912997 2 10/03/2018 FEI # 2250051
Ortho Clinical Diagnostics Inc
VITROS 5600 Integrated System, clinical chemistry analyzer 2 08/06/2019 FEI # 1000136573
Ortho Clinical Diagnostics
VITROS 5600 Integrated System, clinical chemistry analyzer 2 08/06/2019 FEI # 1000136573
Ortho Clinical Diagnostics
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