BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TOSHIBA

    MDR report key: 3892493 · Received June 24, 2014

    Report

    Report Number
    2020563-2014-00002
    Event Type
    Injury
    Date Received
    June 24, 2014
    Date of Event
    May 26, 2014
    Report Date
    May 28, 2014
    Manufacturer
    TOSHIBA MEDICAL SYSTEMS CORPORATION
    Product Code
    MQB
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    RADIOLOGIC TECHNOLOGIST

    Narratives

    Additional Manufacturer Narrative · 1

    IT HAS BEEN DETERMINED BY THE MANUFACTURER THAT THE CAUSE OF THIS ISSUE IS USER ERROR. THE OPERATION MANUAL CONTAINS CAUTION STATEMENTS TO BE AWARE OF THE POSITION OF THE CABLE AND STEPPING OR TRIPPING ON THE CABLE MAY RESULT IN PERSONAL INJURY OR IN DAMAGE TO THE CABLE.

    Description of Event or Problem · 1

    TECHNOLOGIST ALLEGEDLY TRIPPED ON THE CABLE THAT CONNECTS TO THE FLAT PANEL DETECTOR CAUSING HIM TO FALL AND BREAK HIS HIP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    367672 TOSHIBA FLUOROSCOPIC X-RAY SYSTEM MQB TOSHIBA MEDICAL SYSTEMS CORPORATION DRAD-3000E

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| O