BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NUTRIFILL

    MDR report key: 22297116 · Received June 20, 2025

    Report

    Report Number
    3016114779-2025-00020
    Event Type
    Injury
    Date Received
    June 20, 2025
    Report Date
    June 20, 2025
    Manufacturer
    ASEPT PAK
    Product Code
    MRC
    UDI-DI
    00850012123002
    PMA / PMN Number
    K181566
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 0

    PATIENT SM INDICATED THAT THEY HAD RECENTLY EXPERIENCED SEVERAL EYE ISSUES AND HAD VISITED THEIR DOCTOR TWICE DUE TO EYE INFECTIONS. RED EYE/LIGHT SENSITIVITY TREATED FOR AN ABRASION INITIALLY AND THEN FOR "DRY IRRITATED EYES" AND WAS PRESCRIBED ANTIBIOTICS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1669814 NUTRIFILL NUTRIFILL MRC ASEPT PAK HGI 00850012123002

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention