BEUDAMED
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    VIDEOSCOPE "CYF-V2", EUROPEAN VERSION

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FAJ·December 11, 2019

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDT·September 15, 2015

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·January 27, 2011

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDT·November 2, 2015

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·April 7, 2017

    HAMILTON-T1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·May 13, 2025

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·April 3, 2023

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·October 7, 2019

    EVIS EXERA DUODENOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDT·September 28, 2015

    EVIS EXERA DUODENOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDT·September 28, 2015

    COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·September 8, 2023

    PUSH BUTTON PENCIL, EXT.STD. BLADE

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·April 16, 2019

    HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS)

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·March 30, 2023

    UNKNOWN SOLAR ULNA

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDC·January 24, 2023

    MARKED SPRING TIP GUIDEWIRE

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code KNQ·August 30, 2012

    ZILVER 635 BILIARY SELF EXPANDING METAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·December 4, 2024

    ECHELON LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 30, 2015

    POWERPICC PROVENA SOLO 5F TL MAX BARRIER PLUS KIT W/GUARDIVA

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·February 25, 2022

    SPECTRA OPTIA

    FDA Adverse Event
    Malfunction ·TERUMO BCT·Product code LKN·March 19, 2025

    FUSION OMNI-TOME PRE-LOADED SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code KNS·April 3, 2017