BEUDAMED
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    ELECSYS 2010

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS CORP.·Product code JJE·December 13, 2007

    YPSOPUMP INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 3, 2024

    RAD-8, HORIZONTAL

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·October 7, 2016

    JUVEDERM ULTRA PLUS XC/L/DO (VOLUME UNK)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·April 17, 2014

    VITROS CHEMISTRY PRODUCTS TOBRA REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LDO·August 25, 2022

    VITROS CHEMISTRY PRODUCTS TOBRA REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LDO·February 14, 2019

    VITROS CHEMISTRY PRODUCTS TOBRA REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LDO·July 7, 2016

    VITROS CHEMISTRY PRODUCTS TOBRA REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LDO·August 25, 2022

    LIFEPAK 9P DEFIBRILLATOR/MONITOR/PACEMAKER

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL CORP.·Product code LDO·December 4, 1997

    VITROS CHEMISTRY PRODUCTS TOBRA REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code LDO·March 28, 2008

    BARCO

    FDA Adverse Event
    Malfunction ·BARCO NV·Product code DXJ·July 28, 2023

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·November 8, 2021

    ADVIA CENTAUR XPT PSA

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MTF·December 13, 2017

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 23, 2023

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 23, 2023

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·July 21, 2014

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·July 21, 2014

    PEN NEEDLE 32G 4MM 5B XTW 100CT EU

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·April 24, 2025

    ADVIA CENTAUR XPT PROSTATE SPECIFIC ANTIGEN (PSA) ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOTICS, INC·Product code MTF·January 29, 2018

    1053 OTOAIR BLUETOOTH DONGLE

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL DENMARK·Product code EWO·March 7, 2020