BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TROJAN LATEX CONDOM UNSPECIFIED

    MDR report key: 17259267 · Received July 5, 2023

    Report

    Report Number
    2280705-2023-01033
    Event Type
    Injury
    Date Received
    July 5, 2023
    Report Date
    July 3, 2023
    Manufacturer
    CHURCH & DWIGHT CO., INC
    Product Code
    HIS
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    THIS SPONTANEOUS REPORT (2023-CDW-01033, 007800839A) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A CONSUMER (AGE AND GENDER UNSPECIFIED) WHOSE CONDOM BROKE AND DEVELOPED ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS) AFTER USING THE TROJAN LATEX CONDOM UNSPECIFIED. ON AN UNSPECIFIED DATE, THE CONSUMER USED TROJAN LATEX CONDOM UNSPECIFIED. THE CONSUMER ALLEGED THAT THE CONDOM BROKE, AND THE CONSUMER GOT AIDS. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH TROJAN LATEX CONDOM UNSPECIFIED WAS NOT APPLICABLE. THE OUTCOME OF THE EVENT AIDS WAS UNKNOWN. THE OUTCOME OF THE CONDOM BREAKAGE WAS NOT APPLICABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1787919 TROJAN LATEX CONDOM UNSPECIFIED CONDOM HIS CHURCH & DWIGHT CO., INC

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown Other