BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BRAINVIEW QEEG

    MDR report key: 21666016 · Received March 21, 2025

    Report

    Report Number
    MW5167983
    Event Type
    Injury
    Date Received
    March 21, 2025
    Date of Event
    March 13, 2025
    Report Date
    March 13, 2025
    Manufacturer
    UNKNOWN
    Product Code
    OLU
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MY NEIGHBOR HAS A NURSE TO USE A QEEG ON ME AND CAUSED ME TO HAVE BAD NEURO EFFECTS AND THEY KEEP DOING ABUSIVE THINGS. I WAS WANTING THE FDA TO STOP ALLOWING UNLICENSED PEOPLE TO HANDLE THIS TECHNOLOGY BECAUSE THE NURSE USES IT ON ME AGAINST MY WILL AND KEEPS HURTING USING TORTURE AFFECTS FROM THE DEVICE. THEY MADE ME ABOUT TO FAINT SEVERAL TIMES. THEY NEARLY KILLED ME TWICE. THEY ALSO KEEP ATTACKING MY "PROFANITY" WITH IT TRYING TO MAKE ME FEEL I AM GETTING "PROFANITY". THE QEEG HAS ALSO MADE ME WEEK WHERE I CAN'T FEEL MY FULL STRENGTH. THEY KEEP HURTING ME WITH IT AND THAT IS WHY WE SHOULDN'T LET UNLICENSED PEOPLE WITH THIS DEVICE. PLEASE DO SOMETHING ABOUT (B)(6) BECAUSE HE IS USING THIS DEVICE AGAINST MY WILL. PLEASE HELP BEFORE HE KILLS ME. I DON'T HAVE THE PRODUCT MY NEIGHBOR DOES AND HE REFUSES TO TAKE IT OFF ME. (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2100235 BRAINVIEW QEEG NORMALIZING QUANTITATIVE ELECTROENCEPHALOGRAPH SOFTWARE OLU UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR Male Other| R| L| S