BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LEAD APRON

    MDR report key: 108496 · Received July 28, 1997

    Report

    Report Number
    MW1011779
    Event Type
    Malfunction
    Date Received
    July 28, 1997
    Date of Event
    July 28, 1997
    Report Date
    July 28, 1997
    Manufacturer
    BT MEDICAL CO., INC.
    Product Code
    EAJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    LEAD APRONS (12) WERE CONTAMINATED. WHEN TESTED. THE GEIGER COUNTER GAVE A READING OF .5 MR/HR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LEAD APRON LEAD APRON EAJ BT MEDICAL CO., INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA