BEUDAMED
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    1600 SEM AUTOMATIC DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP.·Product code MKJ·December 12, 2003

    SEMS MODEL 700-A

    FDA Adverse Event
    Malfunction ·SOUTHEASTERN MEDICAL·Product code DQA·February 13, 2007

    ALIMAXX-ES ESOPHAGEAL SEM STENT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code ESW·August 22, 2011

    STARBURST XLI ENHANCED SEM-FLEX, 25CM, FLEXIB

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code GEI·May 14, 2010

    ZILVER 635 BILIARY SELF EXPANDING METAL STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·December 5, 2024

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK MEDICAL IRELAND·Product code FGE·June 29, 2023

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·December 11, 2024

    ZILVER 635 SELF-EXPANDING BILIARY STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 24, 2022

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·September 5, 2013

    ZILVER 635 BILIARY SELF EXPANDING METAL STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·November 17, 2022

    ALTA CHANNEL PLT 151MM

    FDA Adverse Event
    Malfunction ·HOWMEDICA, INC.·Product code HRS·January 31, 1997

    NAVITAS CTO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BRIVANT LTD·Product code DQX·March 22, 2011

    ZILVER 635 BILIARY SELF EXPANDING METAL STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·December 6, 2024

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·August 24, 2018

    HUIBREGTSE GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 24, 2022

    COURIER GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BRIVANT LTD·Product code DQX·December 23, 2010

    COURIER GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BRIVANT, LTD.·Product code DQX·August 16, 2010

    SHAVER HP, APSII, HAND CONTROL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·September 20, 2023

    ARMADA 35 PTA CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code LIT·June 3, 2022

    PULSE GEN MODEL 103

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·November 19, 2024