BEUDAMED
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    Filters FDA Adverse Event ×

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

    LIGASURE

    FDA Adverse Event
    Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

    VKMO 11000 #QUADROX-I NEO. MIT RESERVOIR

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·March 27, 2015

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019

    QUADROX-I NEO. MIT RESERVOIR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·April 16, 2015

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021

    OXYGENATOR, CARDIOPULMONARY BYPASS

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 27, 2015

    OXYGENRATOR, CARDIOPULMONARY BYPASS

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 27, 2015

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 2, 2013

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code GFA·May 20, 2011

    GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code MUZ·August 8, 2008

    LIGASURE

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 14, 2021