BEUDAMED
    FDA Adverse Event Death Summary report: N

    NARKOMED

    MDR report key: 673596 · Received February 8, 2006

    Report

    Report Number
    2517967-2006-00029
    Event Type
    Death
    Date Received
    February 8, 2006
    Date of Event
    January 17, 2006
    Report Date
    January 17, 2006
    Manufacturer
    DRAEGER MEDICAL, INC.
    Product Code
    BSZ
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT: WHILE THE PATIENT WAS UNDERGOING AN INTERVENTIONAL RADIOLOGY PROCEDURE, THE PATIENT MOVED, WHILE UNDER GENERAL ANESTHESIA. THIS A S A DELICATE SURGERY AND DUE TO THE MOVEMENT, THE PATIENT CONDITION BECAME CRITICAL AND THEN THE PATIENT EXPIRED. NO REPORTED INFORMATION REGARDING DEVICE PERFORMANCE OR ALARMS.

    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 UNKNOWN Death