BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TROJAN-ENZ

    MDR report key: 881675 · Received July 13, 2007

    Report

    Report Number
    MW5003043
    Event Type
    Malfunction
    Date Received
    July 13, 2007
    Date of Event
    July 10, 2007
    Report Date
    July 13, 2007
    Manufacturer
    CWI CARTER PRODUCTS
    Product Code
    HIS
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I PURCHASED A PACKAGE OF TROJAN LATEX CONDOMS - 36 CT- AND OPENED THE PACKAGE TODAY AND THE EXPIRATION DATE ON ALL OF THE CONDOMS WAS JUNE OF 2005. DIAGNOSIS OR REASON FOR USE: PREVENT PREGNANCY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TROJAN-ENZ NONE HIS CWI CARTER PRODUCTS

    Patients

    Seq Age Sex Outcome Treatment
    1 YR Other