BEUDAMED
    67 results · 33ms · Sources: EU EUDAMED, US FDA

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    QUICKMOVE TRANSFER AID

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code IKX·November 18, 2020

    EVA600EE

    FDA Adverse Event
    Injury ·HANDICARE AB·Product code FSA·September 13, 2016

    EVAEE LIFTS

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code FSA·September 23, 2016

    CARINA350EM

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code FSA·October 10, 2019

    CARINA350EM

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code FSA·November 16, 2020

    CARINA LIFTS

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code FSA·September 13, 2016

    RETURN 7500I

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code FSA·June 8, 2018

    RETURN 7500I

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code FSA·June 8, 2018

    RETURN 7500I

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code FSA·June 8, 2018

    RETURN 7500I

    FDA Adverse Event
    Injury ·HANDICARE AB·Product code IKX·January 10, 2018

    ReTurn 7500/7500 Aid, transfer

    FDA Recall
    Terminated ·Handicare USA, Inc.·Product code IKX·April 15, 2014

    ReTurn 7500/7500 Aid, transfer

    FDA Enforcement
    Class II ·Terminated·Handicare USA, Inc.·November 2, 2016

    ROWALKER

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code ITJ·November 16, 2020

    HANDICARE QUICKMOVE TRANSFER AID

    FDA Adverse Event
    Injury ·HANDICARE AB·Product code IKX·April 8, 2021

    EVA450 EE

    FDA Adverse Event
    Injury ·HANDICARE, AB·Product code FSA·May 1, 2012

    EVA450 EE

    FDA Adverse Event
    Injury ·HANDICARE, AB·Product code FSA·May 1, 2012

    MINILIFT

    FDA Adverse Event
    Injury ·HANDICARE AB·Product code FSA·September 16, 2015

    HANDICARE CARINA 350EM

    FDA Adverse Event
    Injury ·HANDICARE AB·Product code FSA·April 7, 2021

    ROMEDIC

    FDA Adverse Event
    Injury ·HANDICARE AB·Product code FSA·March 15, 2013

    RETURN

    FDA Adverse Event
    Malfunction ·HANDICARE AB·Product code IKX·November 7, 2018