BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    23-2117-0 ANIOSGEL 85 NPC HAND SANITIZ 500ML

    MDR report key: 24114335 · Received January 20, 2026

    Report

    Report Number
    MW5182390
    Event Type
    Malfunction
    Date Received
    January 20, 2026
    Date of Event
    January 6, 2026
    Report Date
    January 12, 2026
    Manufacturer
    ANGELINI PHARMA INC.
    Product Code
    LRJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    A PERITONEAL DIALYSIS (PD) PATIENT CONTACTED TO CUSTOMER SERVICE TO REPORT THAT HAND SANITIZER IS BREAKING HER HANDS OUT AND DRYING THEM OUT AND PEELING. PATIENT CANNOT USE THE HAND SANITIZER. PATIENT DID NOT KNOW WHAT DAY SHE NOTICED THE ISSUE; THE PATIENT INVOLVEMENT WAS UNKNOWN; HOWEVER, THERE WAS NO HARM OR ADVERSE EVENT REPORTED. "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
    175617 23-2117-0 ANIOSGEL 85 NPC HAND SANITIZ 500ML DISINFECTANT, MEDICAL DEVICES LRJ ANGELINI PHARMA INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown