BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEART WARMER

    MDR report key: 26725 · Received July 20, 1995

    Report

    Report Number
    MW4000719
    Event Type
    Malfunction
    Date Received
    July 20, 1995
    Report Date
    March 15, 1995
    Manufacturer
    R.G. BARRY CORP.
    Product Code
    IME
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    LA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE PRODUCT WAS PURCHASED AS A CHRISTMAS GIFT FOR RPTR'S FATHER (ELDERLY). COMPLAINANT HEATED THE PRODUCT FOR APPROX 2 MINUTES & PLACED IT BACK INTO MICROWAVE. AS SHE REMOVED IT FROM MICROWAVE IT EXPLODED & CAUSED SMALL BURNS ON HER KNUCKLES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEART WARMER WARMER IME R.G. BARRY CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 *