BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DRAGER

    MDR report key: 260645 · Received January 30, 2000

    Report

    Report Number
    MW1018033
    Event Type
    Injury
    Date Received
    January 30, 2000
    Date of Event
    January 28, 2000
    Report Date
    January 28, 2000
    Manufacturer
    DRAGER INC.
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Narratives

    Description of Event or Problem · 1

    VENTILATOR WENT INTO APNEA ALARM AND DID NOT VENTILATE PT. NOTHING WAS DONE WITH PT PRIOR TO EVENT TO START THIS AND PT NEEDED TO BE "BUN". THE VENT TAKES 10-15 BREATHS TO SLOWLY BUILD BACK UP TO THE LEVEL OF VENTILATION THAT WAS PREVIOUSLY USED BY THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DRAGER VENT CBK DRAGER INC. EVITA 4 *

    Patients

    Seq Age Sex Outcome Treatment
    1 14 MO Life Threatening| R