BEUDAMED
    FDA Adverse Event Injury Summary report: N

    WECK

    MDR report key: 34343 · Received June 7, 1996

    Report

    Report Number
    34343
    Event Type
    Injury
    Date Received
    June 7, 1996
    Date of Event
    February 27, 1996
    Report Date
    February 28, 1996
    Manufacturer
    XOMED SURGICAL PRODUCTS,INC.
    Product Code
    HNQ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    A PHYSICIAN WAS USING THIS INSTRUMENT DURING EYE SURGERY WHEN HE NOTICED THE INSTRUMENT TIP WAS MISSING. X-RAYS WERE NEEDED OF THE EYE TO DETERMINE WHETHER OR NOT THE TIP COULD BE LOCATED. THE X-RAYS WERE NEGATIVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WECK KUGLEN HOOK HNQ XOMED SURGICAL PRODUCTS,INC. UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Required Intervention