BEUDAMED
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    INRATIO2

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·June 19, 2012

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 30, 2013

    TRANSEND¿ EX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code DQX·May 17, 2012

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·December 30, 2010

    ALARIS® PUMP MODULE

    FDA Adverse Event
    Injury ·CAREFUSION·Product code FRN·January 3, 2020

    MAGELLAN SAFETY NEEDLE 25X5/8 INTL

    FDA Adverse Event
    Malfunction ·TYCO/KENDALL HEALTHCARE·Product code FMI·December 3, 2007

    INRATIO

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC·Product code GJS·April 26, 2011

    INRATIO

    FDA Adverse Event
    Injury ·HEMOSENSE, INC.·Product code GIS·February 6, 2006

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·October 19, 2007

    INRATIO

    FDA Adverse Event
    Injury ·BIOSITE INCORPORATED·Product code JPA·June 23, 2009

    INRATIO ASSY, BOX OF STRIPS, MULTILANGUAGE

    FDA Adverse Event
    Injury ·ALERE SAN DIEGO, INC.·Product code GJS·March 19, 2013

    BD VACUTAINER® NO ADDITIVE (Z) TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 1, 2018

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVE DIVISION·Product code LWR·December 3, 2018

    VANISH POINT TUBERCULIN SYRINGE

    FDA Adverse Event
    Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·December 11, 2007

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·November 17, 2014

    ABL827 FLEX

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code CHL·September 27, 2013

    DURACON ANT CONS TIB INS 11MSM

    FDA Adverse Event
    Injury ·HOWMEDICA INC.·Product code HSH·June 4, 1998

    L3W0900 - AQUACEL AG

    FDA Adverse Event
    Malfunction ·CONVATEC LTD·Product code FRO·January 13, 2022

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVE DIVISION·Product code LWR·December 3, 2018

    ALARIS PUMP MODULE

    FDA Adverse Event
    Injury ·CAREFUSION·Product code FRN·September 3, 2015