BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CANTOR TUBE

    MDR report key: 184543 · Received August 27, 1998

    Report

    Report Number
    48207-1998-00047
    Event Type
    Injury
    Date Received
    August 27, 1998
    Date of Event
    August 11, 1998
    Report Date
    August 26, 1998
    Manufacturer
    WILLY RUSCH AG
    Product Code
    FEI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WHILE ATTEMPTING TO RECONNECT GLASS TUBING TO THE CANTOR TUBE, THE TUBING BROKE-CUTTING NURSE'S INDEX FINGER AND THUMB.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CANTOR TUBE INTESTINAL TUBE FEI WILLY RUSCH AG NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Other