BEUDAMED
    FDA Adverse Event Injury Summary report: N

    WHOOP BAND

    MDR report key: 24431520 · Received February 24, 2026

    Report

    Report Number
    MW5184337
    Event Type
    Injury
    Date Received
    February 24, 2026
    Date of Event
    January 29, 2026
    Report Date
    February 18, 2026
    Manufacturer
    WHOOP INC.
    Product Code
    QDA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I WAS INSTRUCTED BY THE FITNESS COMPANY WHOOP TO KEEP TIGHTENING THE BAND TO ENSURE IT RECORDED MY VITAL SIGNS PROPERLY. UPON DOING SO, THE DEVICE LEFT A RED MARK ON MY SKIN. WHEN I TOLD THE COMPANY ABOUT IT, THEY WANTED TO REPLACE THE BAND. I'VE BEEN WITH THEM FOR OVER 3 YEARS, AND THEY CHARGE $250 PER YEAR FOR THAT? WHAT ARE THE LONG-TERM CONSEQUENCES OF HAVING THAT BAND ON MY ARM?

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    499707 WHOOP BAND ELECTROCARDIOGRAPH SOFTWARE FOR OVER-THE-COUNTER USE QDA WHOOP INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Required Intervention| O BLK SEED.| CREATINE.| K2 AND D3.| MULTIVITAMINS.| PROTEIN.