BEUDAMED
    FDA Adverse Event Summary report: N

    INDICAID HOME COVID TEST

    MDR report key: 16546195 · Received March 15, 2023

    Report

    Report Number
    MW5115749
    Date Received
    March 15, 2023
    Date of Event
    February 18, 2023
    Report Date
    February 21, 2023
    Manufacturer
    PHASE SCIENTIFIC INTERNATIONAL LIMITED
    Product Code
    QKP
    Report Source
    Voluntary report
    Reporter Location
    AL, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    THIS IS NOT ABOUT A VACCINATION. BUT THIS WAS WHAT WAS SENT TO ME TO FILE A COMPLAINT ABOUT THE LOUSY HOME COVID TEST SENT OUT TO MEDICARE PATIENTS AND OTHERS CALLED INDICAID, THESE TEST DO NOT WORK. I TESTED MYSELF WITH ONE ON (B)(6) 2023. DID IT AGAIN TWICE ON (B)(6) 2023. THEN WENT TO THE DOC BECAUSE THE SORE THROAT TOLD ME I HAD COVID. SURE ENOUGH, I TESTED POSITIVE FOR COVID AT THE DOC. CAME HOME AND DID ANOTHER LOUSY INDICAID TEST AND SHOWED NEGATIVE. FOR THE NEXT TWO DAYS I TESTED MYSELF WITH INDICAID AND THEY ALWAYS SAID NEGATIVE. I BOUGHT MY OWN DIFFERENT HOME TESTS AND THEY SHOWED POSITIVE. INDICAID IS A SHAM AND SHOULD NOT BE SENT OUT TO ANYONE. AS I HAVE STATED, I EMAILED TO COMPLAIN ABOUT THE INDICAID COVID HOME TESTS THAT ARE MAILED OUT. THEY EMAILED ME AND TOLD ME TO FILE THIS. THIS HAS NOTHING TO DO WITH A VACCINE. THIS HAS TO DO WITH A HOME TEST THAT DOES NOT WORK AND YOU ARE SENDING THESE OUT TO PEOPLE. I AM POSITIVE FOR COVID. I KEEP TESTING AND IT HAS YET TO SHOW ME POSITIVE AND KEEPS SAYING NEGATIVE. THESE SHOULD NOT BE SENT OUT TO ANYONE. THEY ARE NOT EVEN CLOSE TO BEING ACCURATE. REFERENCE REPORTS MW5115746, MW5115747, MW5115748.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1037592 INDICAID HOME COVID TEST CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM QKP PHASE SCIENTIFIC INTERNATIONAL LIMITED

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR Female