BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TROJAN CONDOMS UNSPECIFIED

    MDR report key: 20307959 · Received September 26, 2024

    Report

    Report Number
    2280705-2024-01489
    Event Type
    Injury
    Date Received
    September 26, 2024
    Report Date
    September 26, 2024
    Manufacturer
    CHURCH & DWIGHT CO.,
    Product Code
    HIS
    Removal / Correction Number
    NOT AVAIL.
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    NOT AVAIL.

    Description of Event or Problem · 0

    THIS SPONTANEOUS REPORT (2024-CDW-01489, 07177586) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A CONSUMER (AGE AND GENDER UNSPECIFIED) WHO DEVELOPED AN ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS) AFTER USING THE TROJAN CONDOMS UNSPECIFIED. ON AN UNSPECIFIED DATE, THE CONSUMER INITIATED TROJAN CONDOMS UNSPECIFIED. AFTER USING THE CONDOM (DEVICE INEFFECTIVE), THE CONSUMER DEVELOPED AN ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS). NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH TROJAN CONDOMS UNSPECIFIED WAS NOT APPLICABLE. THE OUTCOME OF THE EVENT AIDS WAS UNKNOWN. THE OUTCOME OF THE EVENT USED A TROJAN CONDOM AND GOT AIDS WAS NOT APPLICABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1098259 TROJAN CONDOMS UNSPECIFIED CONDOM HIS CHURCH & DWIGHT CO., NOT AVAIL. NOTAVAIL

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other