BEUDAMED
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    ORTHO CLINICAL DIAGNOSTICS

    FDA Adverse Event
    Other ·*·Product code KSZ·August 25, 2005

    ORTHO-CLINICAL DIAGNOSTICS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·August 24, 2006

    ORTHO CLINICAL DIAGNOSTICS

    FDA Adverse Event
    Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·July 27, 2017

    ORTHO-CLINICAL DIAGNOSTICS AUTOWASH 96

    FDA Adverse Event
    Other ·TECAN AUSTRIA GES M.B.H.·Product code IFP·April 21, 2005

    ORTHO CLINICAL DIAGNOSTICS AUTOWEEH 96

    FDA Adverse Event
    Other ·TECAN AUSTRIA GES.M.B.H.·Product code JQW·February 15, 2005

    ORTHO-CLINICAL DIAGNOSTICS AUTOWASH 96

    FDA Adverse Event
    Malfunction ·TECAN AUSTRIA GES.M.B.H·Product code LXG·August 19, 2005

    ORTHO-CLINICAL DIAGNOSTICS MODEL 120 INCUBATOR

    FDA Adverse Event
    Other ·FAIRWAY MEDICAL TECHNOLOGIES·Product code JTQ·November 29, 2006

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 10, 2009

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 10, 2009

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 10, 2009

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 7, 2010

    SURGISCREEN

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·October 5, 2009

    0.8% RESOLVE PANEL B

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·January 14, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·January 11, 2010

    0.8% SELECTOGEN

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 7, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·October 5, 2009