BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GLIDESCOPE 10 HDMI CABLE

    MDR report key: 19250176 · Received May 3, 2024

    Report

    Report Number
    MW5154546
    Event Type
    Injury
    Date Received
    May 3, 2024
    Date of Event
    April 30, 2024
    Report Date
    May 1, 2024
    Manufacturer
    VERATHON INC.
    Product Code
    CCW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    GLIDESCOPE FAILED DURING ACLS (ADVANCED CARDIAC LIFE SUPPORT). SCREEN DISPLAY WAS TOTALLY BLACK. ISSUE IDENTIFIED AS BENT PINS AT HDMI CABLE CONNECTION. RESUSCITATION MAINTAINED WITH CONTINUOUS VENTILATION AND PATIENT INTUBATED BY DIRECT LARYNGOSCOPY. AIRWAY CONFIRMED WITH AUSCULTATION AND CO2 (CARBON DIOXIDE) DETECTOR. A SECOND GLIDESCOPE OBTAINED BY RESPIRATORY STAFF AND FOUND TO BE IN WORKING ORDER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    642683 GLIDESCOPE 10 HDMI CABLE LARYNGOSCOPE, RIGID CCW VERATHON INC. GLIDESCOPE CORE

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Male Required Intervention