BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BAUSCH & LOMB, INC.

    MDR report key: 3265755 · Received June 3, 2013

    Report

    Report Number
    3265755
    Event Type
    Injury
    Date Received
    June 3, 2013
    Date of Event
    May 8, 2013
    Report Date
    June 3, 2013
    Manufacturer
    *
    Product Code
    LPL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    ME, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    245361 BAUSCH & LOMB, INC. INTRAOCULAR LENS LPL * L122UV *

    Patients

    Seq Age Sex Outcome Treatment
    1 36 YR Hospitalization| R