BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SOFPORT INTRAOCULAR LENS

    MDR report key: 4203030 · Received October 23, 2014

    Report

    Report Number
    1119279-2014-00251
    Event Type
    Injury
    Date Received
    October 23, 2014
    Date of Event
    August 18, 2014
    Report Date
    September 26, 2014
    Manufacturer
    BAUSCH & LOMB, INC.
    Product Code
    HQL
    PMA / PMN Number
    P910061
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE WAS RECEIVED FOR EVALUATION. INVESTIGATION OF THIS EVENT IS IN PROGRESS. A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT DURING LENS INSERTION THE LENS BENT. THE INCISION WAS ENLARGED TO REMOVE THE LENS AND ANOTHER LENS WAS IMPLANTED. SUTURES WERE PLACED. PLEASE REFERENCE MDR # 1119279-2014-00252 FOR THE INSERTER USED IN THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    674904 SOFPORT INTRAOCULAR LENS INTRAOCULAR LENS HQL BAUSCH & LOMB, INC. LI61SE 4370228

    Patients

    Seq Age Sex Outcome Treatment
    1 Other EZ-28 DELIVERY DEVICE