BEUDAMED
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    IMMAGE® IMMUNOCHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code NQD·February 3, 2012

    COBAS 6000 C501MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·November 29, 2010

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·January 19, 2011

    CARDIAC C-REACTIVE PROTEIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·July 24, 2011

    CARDIAC C-REACTIVE PROTEIN (LATEX) HIGH SENSITIVE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·July 31, 2025

    COBAS 6000 C501MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·January 6, 2011

    CRPHS CARDIAC C-REACTIVE PROTEIN (LATEX) HIGH SENSITIVE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·November 15, 2016

    COBAS 6000

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·November 30, 2007

    CRPHS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·November 20, 2023

    SYNCHRON SYSTEMS HIGH SENSITIVITY CARDIAC C-REACTIVE PROTEIN (CRPH) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code NQD·October 25, 2011

    LX PRO HIGH SENSITIVITY CRP

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code NQD·April 21, 2011

    IMMAGE® 800 IMMUNOCHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code NQD·September 6, 2012

    CARDIAC C-REACTIVE PROTEIN (LATEX) HIGH SENSITIVE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·December 6, 2024

    ATELLICA CH

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code NQD·April 11, 2025

    CRPHS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·October 19, 2023

    CRPHS CARDIAC C-REACTIVE PROTEIN (LATEX) HIGH SENSITIVE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·July 17, 2017

    CRPHS CARDIAC C-REACTIVE PROTEIN (LATEX) HIGH SENSITIVE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NQD·February 26, 2021

    CRP LATEX REAGENT

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code NQD·March 18, 2021

    Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus CS analyzer Catalog Number: CCCRP-C SMN:10445067

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics Inc·Product code NQD·November 11, 2015

    Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus CS analyzer Catalog Number: CCCRP SMN:10445066

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics Inc·Product code NQD·November 11, 2015