BEUDAMED
    FDA Adverse Event Other Summary report: N

    TOSHIBA

    MDR report key: 533322 · Received March 2, 2004

    Report

    Report Number
    2020563-2004-00002
    Event Type
    Other
    Date Received
    March 2, 2004
    Date of Event
    February 11, 2004
    Report Date
    March 2, 2004
    Manufacturer
    TOSHIBA MEDICAL SYSTEMS CORPORATION
    Product Code
    LNH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    MAGNET QUENCHED DURING SERVICE ACTIVITIES. HELIUM GAS WAS DISCHARGED INTO FACILITY WITH NO INJURY TO STAFF OR PTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOSHIBA SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING LNH TOSHIBA MEDICAL SYSTEMS CORPORATION MRT1501/P2 *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA