BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CANNON

    MDR report key: 2415046 · Received January 9, 2012

    Report

    Report Number
    MW5023787
    Event Type
    Injury
    Date Received
    January 9, 2012
    Date of Event
    January 9, 2012
    Report Date
    January 9, 2012
    Manufacturer
    CANON U.S.A. INC.
    Product Code
    IZL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PORTABLE X-RAY HAD UN-COMMANDED AND UNCONTROLLED MOVEMENT. PORTABLE SPUN UNCONTROLLED INJURING A X-RAY TECHNICIAN, (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CANNON PORTABLE X-RAY IZL CANON U.S.A. INC. RADPRO 40KW

    Patients

    Seq Age Sex Outcome Treatment
    1