BEUDAMED
    FDA Adverse Event Other Summary report: N

    ACRYSOF

    MDR report key: 274815 · Received April 20, 2000

    Report

    Report Number
    1119421-2000-00358
    Event Type
    Other
    Date Received
    April 20, 2000
    Report Date
    March 20, 2000
    Manufacturer
    ALCON LABORATORIES, INC
    Product Code
    HQL
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    A SURGEON REPORTS THAT A PT HAS SYMPTOMS DESCRIBED AS GLARE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other