BEUDAMED
    FDA Adverse Event Injury Summary report: N

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

    MDR report key: 23862907 · Received December 22, 2025

    Report

    Report Number
    MW5180874
    Event Type
    Injury
    Date Received
    December 22, 2025
    Date of Event
    December 12, 2025
    Report Date
    December 16, 2025
    Manufacturer
    ANGELINI PHARMA INC.
    Product Code
    LRJ
    Adverse Event
    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 THE SILK TAPE MAKES HER BREAKOUT WITH RASHES AND SHE DOES NOT NEED ANYTHING REPLACED, 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
    1875704 23-2117-0 ANIOSGEL 85 NPC HAND SANITIZER 500ML DISINFECTANT, MEDICAL DEVICES LRJ ANGELINI PHARMA INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown