BEUDAMED
    FDA Adverse Event Other Summary report: N

    ACRYSOF

    MDR report key: 245339 · Received October 15, 1999

    Report

    Report Number
    1119421-1999-01853
    Event Type
    Other
    Date Received
    October 15, 1999
    Report Date
    September 17, 1999
    Manufacturer
    ALCON LABORATORIES
    Product Code
    HQL
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    A SURGEON STATES THAT POST CATARACT SURGERY AND INTRAOCULAR LENS (IOL) IMPLANT, PT REPORTS SEEING REFLECTIONS AND DARK ARCS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACRYSOF Implant INTRAOCULAR LENS HQL ALCON LABORATORIES MA30BA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other