BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AIRTRAQ SP

    MDR report key: 21240605 · Received January 27, 2025

    Report

    Report Number
    MW5165214
    Event Type
    Injury
    Date Received
    January 27, 2025
    Date of Event
    September 17, 2024
    Report Date
    January 19, 2025
    Manufacturer
    PRODOL MEDITEC S.A.
    Product Code
    CCW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    CREW PERFORMED A DRUG ASSISTED INTUBATION USING AIRTRAQ VIDEO LARYNGOSCOPE. DURING THIS MORNINGS AMBULANCE CHECK THE AIRTRAQ BATTERY LIFE WAS AT 100 MIN. WE WENT ON A CALL AND ATTEMPTED TO INTUBATE THE PATIENT. ORIGINALLY THE AIRTRAQ BATTERY WAS READING 100 MIN AND WITHIN 30 SECONDS THE BATTERY WENT DOWN TO 0%. WHILE TRYING TO TROUBLE SHOOT (POWER OFF AND BACK ON) THE BUTTONS ON THE SCREEN WERE FROZEN AND NOT REGISTERING FINGER TOUCHES. DEVICE WAS UNABLE TO BE POWERED OFF. CREWS PLACED A RESCUE AIRWAY. ROSC OBTAINED. AFTER THE CALL THE CREW TOOK A LOOK AT THE AIRTRAQ DEVICE AND NOTICED THE BATTERY LIFE WAS NOW READING 71 MIN BATTERY LIFE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1607204 AIRTRAQ SP LARYNGOSCOPE, RIGID CCW PRODOL MEDITEC S.A. SP

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR Female Hospitalization| R