BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VITRAX

    MDR report key: 10739 · Received January 3, 1994

    Report

    Report Number
    MW1000266
    Event Type
    Injury
    Date Received
    January 3, 1994
    Report Date
    December 13, 1993
    Manufacturer
    ALLERGAN MEDICAL OPTICS
    Product Code
    LZP
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    POST OPERATIVE CORNEAL EDEMA, UVEITIS, PROTRACTED RECOVERY OF VISION FOLLOWING CATARACT REMOVAL WITH IOL IRRITATION BY PHACOEMULSIFICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VITRAX INTRAOCULAR VISCOELASTIC LZP ALLERGAN MEDICAL OPTICS

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Required Intervention