BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AIRLIFE CPAP DRIVER

    MDR report key: 1183125 · Received October 1, 2008

    Report

    Report Number
    1183125
    Event Type
    Malfunction
    Date Received
    October 1, 2008
    Report Date
    October 1, 2008
    Manufacturer
    CARDINAL HEALTH MEDICAL PRODUCTS & SERVICES
    Product Code
    BZD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    FL, US

    Narratives

    Description of Event or Problem · 1

    NURSE ELECTIVELY EXTUBATED HER PT TO NCPAP. PT PLACED ON AIRLIFE CPAP DRIVER. IT WAS FUNCTIONING AT FIRST, BUT THEN IT BEGAN POWERING DOWN AND RESTARTED THREE TIMES. THE DEVICE WAS REMOVED FROM PT AND REPLACED WITH ANOTHER ONE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AIRLIFE CPAP DRIVER VENTILATOR, CPAP BZD CARDINAL HEALTH MEDICAL PRODUCTS & SERVICES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 3 MO