BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 2040625 · Received March 22, 2011

    Report

    Report Number
    1720753-2011-02626
    Event Type
    Malfunction
    Date Received
    March 22, 2011
    Date of Event
    February 28, 2011
    Report Date
    March 22, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ON SITE INVESTIGATION. THE HIGH VOLTAGE CABLE WAS CLEANED AND REGREASED 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 THAT THE 9900 SYSTEM MADE A POPPING NOISE FROM THE X-RAY TUBE DURING A CASE. THE SYSTEM SHUT DOWN HAD TO BE REBOOTED THEN THE PROCEDURE WAS COMPLETED. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1