BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEUROFEEDBACK

    MDR report key: 5466482 · Received February 24, 2016

    Report

    Report Number
    MW5060572
    Event Type
    Injury
    Date Received
    February 24, 2016
    Date of Event
    February 24, 2016
    Report Date
    February 24, 2016
    Manufacturer
    EEG INFO
    Product Code
    HCC
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 0

    MY NAME IS (B)(6) I HAVE BOUGHT THIS DEVICE NEUROFEEDBACK FROM (B)(6). THIS COMPANY "CLAIMS LIES", FILTERS NEGATIVE REVIEWS, THREATENS THOSE WHO SPEAK OUT. THEY SOLD THE DEVICE WITHOUT A PRESCRIPTION. MISBRANDING LEADING TO SERIOUS DISABLING ADVERSE EFFECTS, SEVERE MEMORY AND COGNITIVE IMPAIRMENT. EEG TESTING "AMIABLE" HARMING ABILITY TO FUNCTION LEADING TO TICKS AND ACADEMIC DISMISSAL. WORSE, THEY REFUSE TO FIX IT! I AM WILLING TO SIT AND MONITOR MY CONDITIONS. THEY TRY TO RAISE PUBLIC AGAINST FDA AND (B)(6) THAT THIS DEVICE IS SAFE. THIS DEVICE IS DANGEROUS, I HAD IT. I HAD 300 SESSIONS, EVEN MORE DRUGS I TAKE NOW TO WARD OFF ITS ADVERSE EFFECT. "IS NOT HELPING". THIS COMPANY, IS A SCAM THEY DO, FROM WASTE ABUSE AS WELL AS SCAMMING VETERANS. WHAT CAN YOU DO, IT RUINS MY LIFE. THEY SEND THREATS EVERY TIME I POST TO (B)(6) AND THEY USE THEIR EMPLOYEES TO PUT FAKE REVIEWS ON THEIR SITE AND SOME OTHER SITE. THEY ARE CRIMINALS AND YOU CAN USE MY RESULT TO RECALL THIS DEVICE AND SEIZE THEM. I AM PROOF OF INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    112658 NEUROFEEDBACK NEUROFEEDBACK HCC EEG INFO

    Patients

    Seq Age Sex Outcome Treatment
    0 31 YR Other| R| S WELLBUTRIN IS NO LONGER