BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8800

    MDR report key: 2100257 · Received May 16, 2011

    Report

    Report Number
    9617766-2011-01056
    Event Type
    Malfunction
    Date Received
    May 16, 2011
    Date of Event
    May 6, 2011
    Report Date
    May 16, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REPRESENTATIVE PERFORMED AN ONSITE INVESTIGATION. THE CMOS SETTINGS WERE RECONFIGURED. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND PUT BACK INTO SERVICE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM WOULD NOT BOOT UP AND THE MONITOR'S GREEN LIGHT CAME ON BUT THE MONITOR WOULD NOT POWER UP. THE SYSTEM DISPLAYED CMOS ERROR MESSAGES. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 8800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 8800

    Patients

    Seq Age Sex Outcome Treatment
    1