BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9600

    MDR report key: 2062059 · Received April 6, 2011

    Report

    Report Number
    1720753-2011-03279
    Event Type
    Malfunction
    Date Received
    April 6, 2011
    Date of Event
    March 18, 2011
    Report Date
    April 6, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE MFR'S SERVICE REP PERFORMED AN ON-SITE INVESTIGATION. THE SERVICE REP REPLACED THE SRAM. THE SYSTEM WAS TESTED AND OPERATES AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE 9600 SYSTEM DISPLAYED A SOFTWARE CORRUPTION ERROR MESSAGE. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9600 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9600

    Patients

    Seq Age Sex Outcome Treatment
    1