BEUDAMED
    FDA Adverse Event Other Summary report: N

    GE/DATE OHMEDA

    MDR report key: 1019970 · Received March 27, 2008

    Report

    Report Number
    MW5006016
    Event Type
    Other
    Date Received
    March 27, 2008
    Date of Event
    February 28, 2008
    Report Date
    March 10, 2008
    Manufacturer
    G.E. REPAIR SERVICE CENTER
    Product Code
    BSZ
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    WHILE BEING USED ON THE PT, EQUIPMENT EMANATED A BURING SMELL; NO SMOKE, FLAME, DEBRIS WERE OBSERVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE/DATE OHMEDA CARDIO CAPS BSZ G.E. REPAIR SERVICE CENTER 6051-0000-164-01

    Patients

    Seq Age Sex Outcome Treatment
    1 5 MO