BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 3982743 · Received July 24, 2014

    Report

    Report Number
    1720753-2014-06354
    Event Type
    Malfunction
    Date Received
    July 24, 2014
    Date of Event
    July 8, 2014
    Report Date
    July 25, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC0
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REPRESENTATIVE PERFORMED AN ON SITE INVESTIGATION. THE GENERATOR BATTERY WAS REPLACED AND THE HIGH VOLTAGE CABLE WAS CLEANED AND GREASED DURING THE SERVICE CALL. 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 CHARGER FAILED MESSAGES, KV ON IN ERRORS, AND HEARING A LOUD BANG AT TIME OF ERROR. THIS RESULTED IN AN INTERMITTENT, RECOVERABLE LOSS OF IMAGING FUNCTIONALITY. THIS COULD CAUSE PROCEDURAL DELAYS. THERE IS NO REPORT OF INJURY OR DEATH ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    434999 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC0 9900

    Patients

    Seq Age Sex Outcome Treatment
    1