BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VIBRATION PLATE

    MDR report key: 24832797 · Received April 9, 2026

    Report

    Report Number
    MW5186578
    Event Type
    Injury
    Date Received
    April 9, 2026
    Date of Event
    March 14, 2026
    Report Date
    April 6, 2026
    Manufacturer
    UNK
    Product Code
    LLN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PRODUCT: VIBRATION PLATE (MARKETED TO INCREASE CORE STRENGTH, IMPROVE BALANCE, AND STABILITY) BRAND/MODEL: POWER PLATE, 71-MOV-3600 ASIN: (B)(4). DATE OF INCIDENT:(B)(6) 2026. INCIDENT DESCRIPTION: A CUSTOMER REPORTED THAT UPON FIRST USE OF THE PRODUCT, IMMEDIATELY AFTER PLUGGING THE UNIT INTO A WALL OUTLET, THEY EXPERIENCED A WHINING NOISE AND A BURNING SMELL EMANATING FROM THE UNIT. THE CUSTOMER BRIEFLY CONTINUED USE THINKING IT MAY BE NORMAL FOR A NEW PRODUCT BUT SHUT IT OFF WHEN THE BURNING SMELL INTENSIFIED. WHILE ATTEMPTING TO UNPLUG THE UNIT FROM THE WALL OUTLET, THE CUSTOMER SUSTAINED BURNS TO TWO FINGERTIPS. THE CUSTOMER SOUGHT TREATMENT AT AN EMERGENCY ROOM. THIS WAS THE PRODUCT'S FIRST USE. LOCATION OF USE WAS NOT SPECIFIED IN THE CUSTOMER'S REPORT. ACTIONS TAKEN TO DATE: PRODUCT HAS BEEN REMOVED FROM SALE. CUSTOMER HAS BEEN ADVISED TO PRESERVE THE UNIT, PACKAGING, AND ALL ACCESSORIES. CUSTOMER HAS BEEN DIRECTED TO AMAZON'S PROPERTY DAMAGE AND PERSONAL. INJURY CLAIMS PROCESS INTERNAL SAFETY REVIEW HAS BEEN INITIATED. PLEASE ADVISE ON NEXT STEPS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    620137 VIBRATION PLATE DEVICE, VIBRATION THRESHOLD MEASUREMENT LLN UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention