BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LEAD APRON

    MDR report key: 105804 · Received July 15, 1997

    Report

    Report Number
    MW1011688
    Event Type
    Malfunction
    Date Received
    July 15, 1997
    Report Date
    July 15, 1997
    Manufacturer
    ALIMED INC
    Product Code
    EAJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AR, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    SHIELDING PRODUCTS CONTAIN CONTAMINATED LEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LEAD APRON LEAD APRON EAJ ALIMED INC * *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA