BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 1980124 · Received January 24, 2011

    Report

    Report Number
    1720753-2011-00551
    Event Type
    Malfunction
    Date Received
    January 24, 2011
    Date of Event
    January 6, 2011
    Report Date
    January 24, 2011
    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 REPRESENTATIVE EVALUATED THE SYSTEM AND REPLACED THE HARD DRIVE AND GPOS SINGLE BOARD COMPUTER, AND RELOADED SYSTEM SOFTWARE. NO PATIENT INJURY WAS REPORTED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE WORKSTATION WOULD NOT BOOT UP. NO PATIENT 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