BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ORAQUICK

    MDR report key: 24702066 · Received March 26, 2026

    Report

    Report Number
    MW5185958
    Event Type
    Malfunction
    Date Received
    March 26, 2026
    Date of Event
    March 21, 2026
    Report Date
    March 22, 2026
    Manufacturer
    ORASURE TECHNOLOGIES, INC.
    Product Code
    QSS
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    FAKE HIV TEST PUT ON SHELF AT WALMART IN (B)(6). LOT NUMBERS AND REFERENCE NUMBERS DO NOT MATCH AS WELL AS TRADEMARK LOGO ON PACKET THAT STICK COMES IN WHICH I BELIEVE GAVE ME A FALSE NEGATIVE RESULT WHICH CAN LEAD TO INFECTING OTHER INDIVIDUALS DUE TO INACCURATE RESULTS. I LET WALMART KNOW OF THE ISSUE BECAUSE THERE WASN'T A LEGIT PRICE CODE ON THE SHELF EITHER. EVERYTHING ABOUT THE TESTS WAS SUSPICIOUS. I HAVE BEEN UNDER INVESTIGATION AND THESE MEN THREATENED TO INFECT MY KIDS WITH HIV AS WELL AS MYSELF. I WAS INJECTED WITH BLOOD TWICE BY TWO SEPARATE MEN. I BELIEVE THAT'S WHY THESE WERE PUT ON THE SHELF TO FALSIFY MY RESULTS SO I DON'T REPORT IT TO POLICE THAT I WAS INJECTED. THE TWO MEN I BELIEVE WORK FOR THE INVESTIGATORS BUT I DIDN'T KNOW AT THE TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    756382 ORAQUICK HIV SELF-TESTS QSS ORASURE TECHNOLOGIES, INC. 0006722772

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR Female