BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ANIOSGEL 85 NPC HAND SANITIZ 500ML

    MDR report key: 24399738 · Received February 19, 2026

    Report

    Report Number
    MW5184128
    Event Type
    Injury
    Date Received
    February 19, 2026
    Date of Event
    January 28, 2026
    Report Date
    February 12, 2026
    Manufacturer
    ECOLAB INC.
    Product Code
    LRJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    A PERITONEAL DIALYSIS (PD) PATIENT CONTACTED (B)(6) CUSTOMER SERVICE AND SAID HAND SANITIZER MAKES HER BREAKOUT. ADVISED PATIENT LAST ORDER FOR HAND SANITIZER WAS (B)(6) 2024 AND TO PLEASE CHECK EXPIRATION DATE. PATIENT SAID SHE THOUGHT IT SAID 2025. ADVISED PATIENT TO SPEAK TO REGISTERED NURSE; SHE PROBABLY SHOULDN'T BE USING EXPIRED PRODUCT REPORTING. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    458496 ANIOSGEL 85 NPC HAND SANITIZ 500ML DISINFECTANT, MEDICAL DEVICES LRJ ECOLAB INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown