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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, Version 3.3.1 & below For use in the in vitro quantitative, semi-... 2 12/20/2018 FEI # 1000136573
Ortho-Clinical Diagnostics
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
VITROS 5600 Integrated System- (Refurbished). For use in the in vitro quantitative, semi-quantitati... 2 10/05/2018 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System- For use in the in vitro quantitative, semi-quantitative, and qualitat... 2 05/04/2023 FEI # 2250051
Ortho-Clinical Diagnostics, Inc.
VITROS 5600 Integrated System-For use in the in vitro quantitative, semi-quantitative, and qualitati... 2 10/05/2018 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS Immunodiagnostic Products - TSH Reagent Pack (10758750000227) 1912997 2 10/03/2018 FEI # 2250051
Ortho Clinical Diagnostics Inc
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® 5600 Integrated System -Software V3.3.2 & below Product Code: 6802413 For use in the... 2 05/06/2019 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS® 5600 Integrated System Refurbished-Software V3.3.2 & below Product Code: 6802915 For ... 2 05/06/2019 FEI # 1000136573
Ortho-Clinical Diagnostics
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