BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OXYCODONE URINE TEST

    MDR report key: 5124330 · Received September 28, 2015

    Report

    Report Number
    MW5056784
    Event Type
    Malfunction
    Date Received
    September 28, 2015
    Date of Event
    March 10, 2015
    Report Date
    September 28, 2015
    Product Code
    DJG
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    (B)(4) IS SELLING FALSELY ADVERTISED OXYCODONE URINE TESTS. THESE ARE NOT OXYCODONE TESTS, BUT RATHER GENERAL OPIATE TESTS. IT WILL TEST POSITIVE IF ANY OPIATE IS IN YOUR SYSTEM. (B)(4) WILL NOT ANSWER ANY OF MY MESSAGES, EMAILS OR LETTERS REGARDING THIS ISSUE AND PROVIDED ME WITH AN INCORRECT ADDRESS TO RETURN THIS PRODUCT, WHICH WAS RETURNED TO ME TWICE. LAB TESTS SHOWED NO OXYCODONE IN MY URINE, WHILE (B)(4) TESTS SHOWED OXYCODONE BEING IN MY SYSTEM (AFTER 2+ MONTHS AFTER TAKING AN OXYCODONE TABLET). WHICH IS IMPOSSIBLE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    640447 OXYCODONE URINE TEST OXYCODONE URINE TEST DJG

    Patients

    Seq Age Sex Outcome Treatment
    1 0 YR