BEUDAMED
    FDA Adverse Event Other Summary report: N

    TOSHIBA

    MDR report key: 514980 · Received March 2, 2004

    Report

    Report Number
    2020563-2004-00004
    Event Type
    Other
    Date Received
    March 2, 2004
    Date of Event
    February 2, 2004
    Report Date
    March 2, 2004
    Manufacturer
    TOSHIBA MEDICAL SYSTEMS CORPORATION
    Product Code
    LNH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    A PT WAS SCANNED IN THE SUPINE POSITION USING A LARGE BODY COIL. THE PT'S BARE UPPER ARM WAS IN CONTACT WITH THE COIL DURING SCANNING. IN 2004 THE PT REPORTED TO THE HOSP WITH BURNS ON THEIR THUMB AND THIGH. NO TREATMENT WAS REQUIRED FOR THE BURNS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOSHIBA SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING LNH TOSHIBA MEDICAL SYSTEMS CORPORATION MRT1501/Q3 *

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR Other