BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FLYNN SCLERAL DEPRESSOR

    MDR report key: 288231 · Received August 2, 2000

    Report

    Report Number
    1932180-2000-00005
    Event Type
    Injury
    Date Received
    August 2, 2000
    Date of Event
    July 17, 2000
    Report Date
    July 28, 2000
    Manufacturer
    BAUSCH & LOMB SURGICAL
    Product Code
    HNX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING SURGERY, THE INSTRUMENT HAD A ROUGH EDGE AND CUT THE PT'S EYE. OINTMENT WAS APPLIED TO THE EYE. THERE HAS BEEN NO REPORT OF ADD'L INJURY AS A RESULT OF THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLYNN SCLERAL DEPRESSOR OPHTHALMIC DEPRESSOR HNX BAUSCH & LOMB SURGICAL NA *

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Other