BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ALWAYS MAXI

    MDR report key: 23415913 · Received October 29, 2025

    Report

    Report Number
    MW5178196
    Event Type
    Injury
    Date Received
    October 29, 2025
    Date of Event
    October 21, 2025
    Manufacturer
    UNK
    Product Code
    HHL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    USED ALWAYS BRAND PADS (LARGE SIZE). I USED PAD IN PREPARATION FOR A POTENTIAL PERIOD CYCLE (IMPORTANT TO NOTE I WAS NOT BLEEDING AND HAD NO ABNORMAL CONTACT WITH MY GENITALIA INCLUDING NO INTERCOURSE, EXTERNAL PRODUCTS USED, OR CHANGE IN SOAPS OR DETERGENTS). I LEFT THE PAD ON FOR ABOUT 8 HOURS OVERNIGHT AND IN THE MORNING UPON TAKING IT OFF, I STARTED TO FEEL AN ITCHING BURNING SENSATION ALMOST IMMEDIATELY. OVER THE NEXT FIVE DAYS, SYMPTOMS HAVE INCREASED TO INTENSE BURNING AND ITCHING SENSATIONS ALONG THE ENTIRE GENITALIA. MENSTRUAL CYCLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1541101 ALWAYS MAXI PAD, MENSTRUAL, SCENTED HHL UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Female FLUVOXIMINE.| INSULIN (NOVOLOG), | INSULIN PUMP (OMNIPOD),