BEUDAMED
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    Filters Status: Malfunction ×

    VANISHPOINT

    FDA Adverse Event
    Malfunction ·RETRACTABLE TECHNOLOGIES·Product code RET·May 9, 2008

    COULTER® LH 780

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·September 26, 2011

    COULTER® LH 780

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·September 26, 2011

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·September 21, 2011

    VALLEYLAB

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GEI·November 4, 2025

    VALLEYLAB

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GEI·November 4, 2025

    VALLEYLAB

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GEI·November 4, 2025

    IBD MODERATE RET

    FDA Adverse Event
    Malfunction ·SUNSTAR AMERICAS INC.·Product code EFW·June 2, 2022

    PARSONNET EPICARDIAL RET

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code DWS·May 6, 2020

    HISTOCORE PELORIS 3 RAPID TISSUE PROCESSOR

    FDA Adverse Event
    Malfunction ·LEICA BIOSYSTEMS MELBOURNE PTY. LTD·Product code IEO·June 23, 2022

    STABILITY PIN RET BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code GAD·June 12, 2014

    STABILITY PIN RET BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code GAD·May 1, 2014

    FAVALORO-MORSE STERN RET

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code MDM·December 22, 2009

    N20 SPHERIC RET SUPER

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HQA·July 29, 2020

    STABILITY PIN RET BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code GAD·September 3, 2025

    STABILITY PIN RET BLADE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code GAD·September 8, 2025

    ELECSYS 2010 DISK RET

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 8, 2008

    2010 RACK ELECSYS RET

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 7, 2008

    FORCETRIADZE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GEI·February 3, 2026

    HEX DRIVER, 4.0 CANN/RET

    FDA Adverse Event
    Malfunction ·ORTHOTECH·Product code HXX·February 13, 2012