BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HERO MIGHTY PATCHES UNSPECIFIED

    MDR report key: 20267732 · Received September 20, 2024

    Report

    Report Number
    2280705-2024-01441
    Event Type
    Injury
    Date Received
    September 20, 2024
    Report Date
    September 20, 2024
    Manufacturer
    CHURCH & DWIGHT CO.,
    Product Code
    NAD
    Removal / Correction Number
    NOT AVAIL.
    Adverse Event
    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-01441, (B)(6) FROM THE UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND WAS REPORTED BY A MALE CONSUMER (AGE 20-22) WHO NOTICED A PERMANENT SPOT AFTER USING THE HERO MIGHTY PATCHED UNSPECIFIED. ON AN UNSPECIFIED DATE, THE CONSUMER INITIATED HERO MIGHTY PATCHES UNSPECIFIED TOPICALLY TO HELP WITH ACNE. AFTER USING ONE OF THE PATCHES, HE NOTICED A PERMANENT SPOT AND STOPPED USING IT. HE DID NOT SEEK MEDICAL ATTENTION. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH HERO MIGHTY PATCHES UNSPECIFIED WAS NOT APPLICABLE. THE OUTCOME OF THE EVENT WAS NOT RECOVERED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1525776 HERO MIGHTY PATCHES UNSPECIFIED DRESSING, WOUND, OCCLUSIVE NAD CHURCH & DWIGHT CO., NOT AVAIL. NOT AVAIL.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male Other