BEUDAMED
    FDA Adverse Event Other Summary report: N

    COVIDIEN/MEDTRONIC VENTILATOR

    MDR report key: 21587013 · Received March 12, 2025

    Report

    Report Number
    MW5167599
    Event Type
    Other
    Date Received
    March 12, 2025
    Date of Event
    February 26, 2025
    Report Date
    March 9, 2025
    Manufacturer
    COVIDIEN/MEDTRONIC
    Product Code
    CBK
    Report Source
    Voluntary report
    Reporter Location
    CO, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    WHILE VENTILATOR WAS ON THE PATIENT, THE NUMBERS FOR VOLUME ON THE SCREEN DISAPPEARED, BUT THE VENTILATOR WAS STILL GIVING BREATHS TO THE PATIENT. THE VENTILATOR WAS CHANGED OUT WITH ANOTHER ONE AND AN ABG 30 MINUTES LATER SHOWED NO CHANGE IN THE PATIENT'S BASELINE ABGS (ARTERIAL BLOOD GASSES). VENTILATOR SENT TO BIOMED FOR SERVICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1701384 COVIDIEN/MEDTRONIC VENTILATOR VENTILATOR, CONTINUOUS, FACILITY USE CBK COVIDIEN/MEDTRONIC 980

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Male