BEUDAMED
    1,454 results · 61ms · Sources: EU EUDAMED, US FDA

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    CARDINAL HEALTH, INC.

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code FMI·December 26, 2025

    BIRD

    FDA Adverse Event
    Death ·CARDINAL HEALTH 207, INC.·Product code CBK·June 19, 2009

    ARGYLE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code FOS·December 10, 2025

    UNKNOWN PRODUCT-MED

    FDA Adverse Event
    Malfunction ·PR006 PUERTO RICO-ANASCO·Product code GBX·November 17, 2023

    PLEURX, DENVER BIOMEDICAL

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code KDQ·April 14, 2008

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    VIASYS

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 207, INC.·Product code CBK·June 17, 2009

    SENSORMEDICS

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 207, INC.·Product code LSZ·May 28, 2009

    SENSORMEDICS

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 207, INC.·Product code LSZ·April 17, 2009

    SENSORMEDICS

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 207, INC.·Product code LSZ·September 10, 2009

    RAPID ASSAY PIFA HEPARIN PLATELET FACT4

    FDA Adverse Event
    Injury ·CARDINAL HEALTH 200, LLC·Product code LCO·October 16, 2020

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    KANGAROO JOEYPUMP W/POLE CLMP

    FDA Adverse Event
    Injury ·COVIDIEN·Product code LZH·August 9, 2021

    MAGELLAN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code FMI·September 6, 2023

    PENROSE DRAIN 12 X 3 4

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code LRO·April 13, 2011

    CARDINAL HEALTH SAFETY LANCETS LOW FLOW

    FDA Adverse Event
    Malfunction ·OWEN MUMFORD LIMITED·Product code FMK·July 27, 2023

    SENSORMEDICS

    FDA Adverse Event
    Other ·CARDINAL HEALTH 207, INC.·Product code LSZ·September 18, 2009

    ALLEGIANCE SILICONE ELASTOMER COATING

    FDA Adverse Event
    Malfunction ·UNOMEDICAL SDN BHD·Product code KOD·December 7, 2007

    PERSONNA PLUS BLADE, NON-STERILE

    FDA Adverse Event
    Injury ·SOUTHMEDIC INC.·Product code GES·July 13, 2012

    CATHETER SUCT 8FR W/CONTROL COILED

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BSY·January 20, 2012