BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LEAD APRON

    MDR report key: 107880 · Received July 25, 1997

    Report

    Report Number
    MW1011771
    Event Type
    Malfunction
    Date Received
    July 25, 1997
    Date of Event
    July 1, 1997
    Report Date
    July 25, 1997
    Manufacturer
    BURLINGTON MEDICAL SUPPLIES
    Product Code
    EAJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CT, US
    Reporter Occupation
    PHYSICIST

    Narratives

    Description of Event or Problem · 1

    LEAD APRON IS CONTAMINATED. GEIGER METER GAVE A READING OF 400-1600 COUNTS PER MINUTE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LEAD APRON LEAD APRON EAJ BURLINGTON MEDICAL SUPPLIES UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA