BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BACK-AID APRON

    MDR report key: 106074 · Received July 17, 1997

    Report

    Report Number
    MW1011716
    Event Type
    Malfunction
    Date Received
    July 17, 1997
    Date of Event
    July 16, 1997
    Report Date
    July 17, 1997
    Manufacturer
    ALIMED, INC.
    Product Code
    EAJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE LEAD APRON IS CONTAMINATED. THE READING WITH THE GEIGER MUELLER METER WAS .3 MR/HR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BACK-AID APRON LEAD APRON EAJ ALIMED, INC. UNK *
    2 BACK-AID APRON LEAD APRON EAJ ALIMED, INC. UNK *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other