BEUDAMED
    FDA Adverse Event Other Summary report: N

    ACRYSOF

    MDR report key: 1083556 · Received July 25, 2008

    Report

    Report Number
    1119421-2008-00560
    Event Type
    Other
    Date Received
    July 25, 2008
    Date of Event
    January 1, 2008
    Report Date
    June 25, 2008
    Manufacturer
    ALCON RESEARCH , LTD./HUNTINGTON
    Product Code
    HQL
    PMA / PMN Number
    P930014
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE PRODUCT WAS NOT RETURNED FOR ANALYSIS. THE DEVICE REMAINS IMPLANTED. PRODUCT HISTORY RECORDS COULD NOT BE REVIEWED BECAUSE THE REPORTING FACILITY DID NOT PROVIDE A LOT NUMBER OR ANY IDENTIFICATION TRACEABLE TO THE MANUFACTURING DOCUMENTATION. ADDITIONAL INFORMATION HAS BEEN REQUESTED. NO ADDITIONAL INFORMATION HAS BEEN RECEIVED.

    Description of Event or Problem · 1

    A SURGEON REPORTED A PATIENT'S EYESIGHT DECREASED FROM 0.6 TO 0.3 APPROXIMATELY FIVE YEARS FOLLOWING INTRAOCULAR LENS (IOL) IMPLANT SURGERY. THE SURGEON REPORTED, "SOMETHING LIKE GLISTENINGS" WAS OBSERVED IN THE LENS UNDER SLIT LAMP OBSERVATION. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACRYSOF INTRAOCULAR LENS HQL ALCON RESEARCH , LTD./HUNTINGTON MA60BM NI

    Patients

    Seq Age Sex Outcome Treatment
    1 NI Other