BEUDAMED
    FDA Adverse Event Summary report: N

    EYECON

    MDR report key: 12576575 · Received October 4, 2021

    Report

    Report Number
    MW5104390
    Date Received
    October 4, 2021
    Report Date
    November 25, 2020
    Manufacturer
    UNK
    Product Code
    NXB
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    DISPENSED WRONG QUANTITY; (#30 INSTEAD OF #60). MISLABELING. ERROR REACHED PT; NO PT HARM. (B)(6). SUBMISSION ID: (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1464360 EYECON DISPENSER, SOLID MEDICATION NXB UNK

    Patients

    Seq Age Sex Outcome Treatment
    1