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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 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- (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 qualitati... 2 10/05/2018 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Catalog Number 6802413, Unique Device Identifier No. 10758750002740; ... 2 06/06/2016 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Unique Device Identifier No. 10758750002740 & 10758750007110. Intend... 2 04/07/2016 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Chemistry System, Catalog Number 6802413, Unique Device Identifier Number 10758750002740... 2 03/08/2016 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Chemistry System, Catalog Number 6802413, Unique Device Identifier Number 10758750009916... 2 01/13/2016 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 4600 Chemistry System, Software Version 3.2 & Below. Automates pre-analytical and post-ana... 2 06/09/2015 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Chemistry System, Software Version 3.2 & Below. Automates pre-analytical and post-ana... 2 06/09/2015 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, System Product Code 6802413. For use in the in vitro quantitative,... 2 10/16/2014 FEI # 1000136573
Ortho-Clinical Diagnostics
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