BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DUOVISC OVD

    MDR report key: 7613520 · Received June 18, 2018

    Report

    Report Number
    MW5077932
    Event Type
    Injury
    Date Received
    June 18, 2018
    Date of Event
    January 11, 2018
    Report Date
    June 7, 2018
    Manufacturer
    ALCON
    Product Code
    LZP
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    TASS DEVELOPED IN 3 OF 12 CATARACT SURGERIES PERFORMED. DATES OF USE: (B)(6) 2018. IS THE PRODUCT COMPOUNDED: YES. IS THE PRODUCT OVER-THE-COUNTER: NO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    451323 DUOVISC OVD AID, SURGICAL, VISCOELASTIC LZP ALCON

    Patients

    Seq Age Sex Outcome Treatment
    1