BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VISCOAT

    MDR report key: 130462 · Received October 31, 1997

    Report

    Report Number
    2650094-1997-00019
    Event Type
    Injury
    Date Received
    October 31, 1997
    Date of Event
    July 22, 1997
    Report Date
    October 3, 1997
    Manufacturer
    ALCON LABORATORIES, INC.
    Product Code
    LZP
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT WAS MAILED IN TO FDA ON: 12/11/1997.

    Description of Event or Problem · 1

    SURGEON REPORTS PT DID HAVE A CORNEAL TRANSPLANT AND IS DOING WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VISCOAT VISCOELASTIC SOLUTION LZP ALCON LABORATORIES, INC. NA 53613P

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Required Intervention STORZ IOL, BSS