BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 3834476 · Received March 17, 2014

    Report

    Report Number
    1720753-2014-02398
    Event Type
    Malfunction
    Date Received
    March 17, 2014
    Date of Event
    February 17, 2014
    Report Date
    March 17, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REPRESENTATIVE PERFORMED AN ONSITE INVESTIGATION. THE REPORTED ISSUE WAS RESOLVED BY A SYSTEM RE-BOOT. ONSITE INVESTIGATION REVEALED THAT NO CAUSE COULD BE DETERMINED. 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 COLLIMATOR LOCKED UP IN THE CLOSED POSITION. SYSTEM FUNCTIONALITY WAS RECOVERED BY A SYSTEM RE-BOOT. THERE IS NO REPORT OF A PATIENT INJURY OR DEATH ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    157263 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1