BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONNOR WAND

    MDR report key: 200387 · Received December 4, 1998

    Report

    Report Number
    1051791-1998-00001
    Event Type
    Injury
    Date Received
    December 4, 1998
    Date of Event
    October 15, 1998
    Report Date
    November 5, 1998
    Manufacturer
    RHEIN MEDICAL
    Product Code
    HND
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    A PHYSICIAN NOTED THAT THE TIP OF AN INSTRUMENT WAS MISSING AFTER USE DURING EYE SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONNOR WAND OPHTHALMIC SPATULA HND RHEIN MEDICAL 08-07114 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Required Intervention