BEUDAMED
    FDA Adverse Event Other Summary report: N

    FOOT DETOX PAD

    MDR report key: 1013938 · Received March 10, 2008

    Report

    Report Number
    MW5005899
    Event Type
    Other
    Date Received
    March 10, 2008
    Report Date
    March 10, 2008
    Manufacturer
    WISE CHOICE HEALTH, INC.
    Product Code
    MLX
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT PUT THE PAD ON THE BOTTOM OF HER FOOT AND SLEPT WITH IT. UPON REMOVAL, SHE STATED, IT LOOKED LIKE VARICOSE VEIN ALONG WITH PAIN, CRAMPING AND BRUISE. CUSTOMER SAID THAT SHE NEVER HAD VARICOSE VEINS BEFORE. SHE WAS UNABLE TO PROVIDE ANY DEVICE ID NUMBER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FOOT DETOX PAD NONE MLX WISE CHOICE HEALTH, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR