BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SERIES TWENTY THOUSAND LEGACY

    MDR report key: 117974 · Received September 4, 1997

    Report

    Report Number
    2028159-1997-00137
    Event Type
    Injury
    Date Received
    September 4, 1997
    Date of Event
    August 6, 1997
    Report Date
    August 6, 1997
    Manufacturer
    ALCON LABORATORIES, INC.
    Product Code
    HQE
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    REPORTER NOTICED MINUTE CORNEAL BURN AT END OF CASE; USED SUTURE TO CLOSE. PT REPORTED AS DOING WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SERIES TWENTY THOUSAND LEGACY OPHTHALMIC SURGERY SYSTEM HQE ALCON LABORATORIES, INC. STTL UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Required Intervention