BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONTACTS

    MDR report key: 6069143 · Received October 29, 2016

    Report

    Report Number
    MW5065733
    Event Type
    Injury
    Date Received
    October 29, 2016
    Date of Event
    October 25, 2016
    Report Date
    October 29, 2016
    Manufacturer
    UNKNOWN
    Product Code
    LPL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I PURCHASED COSTUME CONTACT LENSES. AFTER TRYING THEM ON THEY CAUSED IRRITATION. I SEARCHED ONLINE TO FIND OUT THE CAUSE, AND DISCOVERED NON PRESCRIPTION CONTACTS ARE ILLEGAL AND DANGEROUS. THE BUSINESS WOULD NOT INITIALLY REFUND THEM, OR RETURN CALL. I FINALLY GOT A RETURN BUT THE BUSINESS IS STILL SELLING THEM SAYING THEY HAVE A LEGAL EXCEPTION TO SELL THEM. I INFORMED THEM THEY CAN EASILY VERIFY ONLINE THAT THIS IS ILLEGAL BY CHECKING SEVERAL GOVERNMENT WEBSITES. I'VE NOT SUCCESSFULLY RETURNED THE PRODUCT, BUT I DO HAVE A RECEIPT, PHONE RECORDING, AND EMAILS REGARDING THE CONTACTS. DISTRIBUTER AURORA OPTICS COMPANY INC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    716727 CONTACTS CONTACTS LPL UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 28 YR Other