BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HYLATOPIC PLUS CREAM

    MDR report key: 23895966 · Received December 26, 2025

    Report

    Report Number
    MW5181201
    Event Type
    Injury
    Date Received
    December 26, 2025
    Date of Event
    December 18, 2025
    Report Date
    December 18, 2025
    Manufacturer
    UNKNOWN
    Product Code
    MGQ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SD, US
    Reporter Occupation
    003
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    PATIENT STATED SHE WAS IN THE HOSPITAL AND FOUND OUT THAT SHE NOW HAS HIGH BLOOD PRESSURE. HER HEALTHCARE PROVIDER HAS NOT BEEN INFORMED YET. NO ADDITIONAL INFORMATION IS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1716022 HYLATOPIC PLUS CREAM DRESSING, WOUND AND BURN, HYDROGEL W/DRUG AND/OR BIOLOGIC MGQ UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR Female