BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GASES USED WITHIN EYE TO PLACE PRESSURE ON DETACHED RETINA

    MDR report key: 23479357 · Received November 5, 2025

    Report

    Report Number
    MW5178552
    Event Type
    Malfunction
    Date Received
    November 5, 2025
    Date of Event
    October 7, 2025
    Report Date
    November 4, 2025
    Manufacturer
    ALCON RESEARCH, LLC.
    Product Code
    LPO
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    C5F8 GAS USED DURING PROCEDURE, MD WAS WORRIED IT CONTRIBUTED TO EYE INFECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2280896 GASES USED WITHIN EYE TO PLACE PRESSURE ON DETACHED RETINA GASES USED WITHIN EYE TO PLACE PRESSURE ON DETACHED RETINA LPO ALCON RESEARCH, LLC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown