BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 3913413 · Received May 14, 2014

    Report

    Report Number
    1720753-2014-04184
    Event Type
    Malfunction
    Date Received
    May 14, 2014
    Date of Event
    May 2, 2014
    Report Date
    May 14, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REPRESENTATIVE PERFORMED AN ONSITE INVESTIGATION. THE POWER SIGNAL INTERFACE PCB AND BATTERY CHARGER PCB WERE EVALUATED AND REPLACED. THE MAINFRAME BATTERY PACKS WERE ALSO REPLACED AND THE F3 FUSE WAS CONFIRMED TO BE OPERATING CORRECTLY. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND RETURNED TO SERVICE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM FAILED TO BOOT TO A USABLE STATE AND EXHIBITED A NON-RECOVERABLE LOSS OF FUNCTIONALITY. NO PT SERIOUS INJURY OR DEATH WAS REPORTED RELATED TO THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    288296 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1