BEUDAMED
    FDA Adverse Event Other Summary report: N

    TOSHIBA

    MDR report key: 315052 · Received February 2, 2001

    Report

    Report Number
    2020563-2001-00001
    Event Type
    Other
    Date Received
    February 2, 2001
    Date of Event
    January 16, 2001
    Report Date
    February 2, 2001
    Manufacturer
    TOSHIBA MEDICAL CO.
    Product Code
    IZF
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    OPERATOR WAS MOVING THE TOMOGRAPHY UNIT WHEN THE TUBE ASSEMBLY SWUNG DOWN AND STRUCK THE PT IN THE HEAD. OPERATOR WAS EVALUATED AND RELEASED BY THE FACILITY EMERGENCY ROOM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    4101 TOSHIBA X-RAY, TOMOGRAPHIC UNIT IZF TOSHIBA MEDICAL CO. XGLA-001A *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other