BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ANTERIOR CHAMBER LENS

    MDR report key: 245163 · Received October 15, 1999

    Report

    Report Number
    1119421-1999-01844
    Event Type
    Injury
    Date Received
    October 15, 1999
    Report Date
    September 17, 1999
    Manufacturer
    ALCON LABORATORIES, INC.
    Product Code
    HQL
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    A SURGEON REPORTS THAT A PT EXPERIENCED AN IRIS HEMORRHAGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ANTERIOR CHAMBER LENS Implant INTRAOCULAR LENS HQL ALCON LABORATORIES, INC. MTA5U0 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention