BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZEM LEAD APRON

    MDR report key: 108487 · Received July 29, 1997

    Report

    Report Number
    MW1011777
    Event Type
    Malfunction
    Date Received
    July 29, 1997
    Date of Event
    July 28, 1997
    Report Date
    July 29, 1997
    Manufacturer
    EZ-EM INCORP.
    Product Code
    EAJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TWO LEAD APRONS WERE FOUND TO BE CONTAMINATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EZEM LEAD APRON LEAD APRON EAJ EZ-EM INCORP. NI NI

    Patients

    Seq Age Sex Outcome Treatment
    1 NA