BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9990

    MDR report key: 3161696 · Received June 3, 2013

    Report

    Report Number
    1720753-2013-06722
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Date of Event
    May 23, 2013
    Report Date
    June 4, 2013
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    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 ONSITE INVESTIGATION. THE HAND SWITCH WAS REPLACED. THE SYSTEM WAS THEN FOUND TO BE OPERATING AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM DISPLAYED AN X-RAY SWITCH STUCK ERROR MESSAGE. THE ERROR MESSAGE COULD NOT BE CLEANED AND THE FLUOROSCOPY FUNCTION WAS DISABLED AS A RESULT. THERE IS NO REPORT OF PATIENT INJURY ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    243629 9990 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1