BEUDAMED
    FDA Adverse Event Other Summary report: N

    NARKOMED

    MDR report key: 289623 · Received August 9, 2000

    Report

    Report Number
    2517967-2000-00037
    Event Type
    Other
    Date Received
    August 9, 2000
    Date of Event
    August 4, 2000
    Report Date
    August 9, 2000
    Manufacturer
    DRAEGER MEDICAL, INC.
    Product Code
    BSZ
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT: AFTER INTUBATION, THE DR INSERTED A NASOGASTRIC TUBE AND APPLIED SUCTION TO IT DURING VENTILATION. AT THAT TIME, THE ANESTHESIA MACHINE DISPLAYED NEGATIVE PRESSURE AND SUB ATMOSPHERIC PRESSURE AND THE MACHINE STOPPED VENTILATING. THE USER ATTEMPTED TO SWITCH TO MANUAL MODE, BUT WAS NOT ABLE TO VENTILATE THE PT. AN AMBU BAG WAS THEN APPLIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NARKOMED ANESTHESIA MACHINE BSZ DRAEGER MEDICAL, INC. 6000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other