BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    APPLE WATCH ECG

    MDR report key: 14788026 · Received June 22, 2022

    Report

    Report Number
    MW5110458
    Event Type
    Malfunction
    Date Received
    June 22, 2022
    Date of Event
    June 13, 2021
    Report Date
    June 19, 2022
    Manufacturer
    APPLE INC.
    Product Code
    QDA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    BR
    Reporter Occupation
    PATIENT
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    MY APPLE DEVICES HAVE HIGH LEVELS OF RADIOFREQUENCY, ALMOST DOUBLE THEE PERMITTED. ON APPLE INC, THEY SHOW MY DEVICES AS ALMOST EXCLUSIVE DEVICES WITH THE SAME PROBLEM. WHY IS THAT? I'M SUFFERING VIRTUAL CRIMES AND SOON DISCOVERED THAT I WAS BEING PART OF STUDIES BEFORE MY CONSENT. I NEED ASSISTANCE. I'M A BRAZILIAN DOCTOR AND LOVE USA, AND HOPE TO GET ANSWERS. THANK YOU. I BELIEVE IT STARTED IN 2017 ON APPLE AND HARVARD'S STUDY INVOLVING ECG ON APPLE WATCHES. FDA SAFETY REPORT ID # (B)(4). .

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1090337 APPLE WATCH ECG ELECTROCARDIOGRAPH SOFTWARE FOR OVER-THE-COUNTER USE QDA APPLE INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Male Other APPLE WATCH| IPAD| IPHONE