BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 4134047 · Received September 26, 2014

    Report

    Report Number
    1720753-2014-08198
    Event Type
    Malfunction
    Date Received
    September 26, 2014
    Date of Event
    September 10, 2014
    Report Date
    September 25, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS(SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ON SITE INVESTIGATION. THE POWER SUPPLY AND POWER SUPPLY CABLE HARNESS WERE EVALUATED AND REPLACED. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND RETURNED TO SERVICE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED AND ERROR INDICATING NO CONNECTION WITH THE CONTROL PANEL. ADDITIONALLY, A COMMUNICATION ERROR WAS DISPLAYED WHICH RESULTED IN NO X-RAYS. THERE IS NO REPORT OF DEATH OR SERIOUS INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    602614 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS(SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1