BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SWEAT PATCH

    MDR report key: 6551188 · Received May 4, 2017

    Report

    Report Number
    MW5069602
    Event Type
    Malfunction
    Date Received
    May 4, 2017
    Date of Event
    February 15, 2017
    Report Date
    May 4, 2017
    Manufacturer
    PHARMCHEM INC
    Product Code
    FMH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I AM CURRENTLY BEING DRUG TESTED WITH THE SWEAT PATCH BY PHARMCHEM. THIS PRODUCT IS EXTREMELY FAULTY, PRODUCING FALSE POSITIVES AND RUINING MY LIFE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    326625 SWEAT PATCH SWEAT PATCH FMH PHARMCHEM INC

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR