BEUDAMED
    FDA Adverse Event Death Summary report: N

    CLINTEC ENTERAL FEEDING TUBE

    MDR report key: 33427 · Received June 12, 1996

    Report

    Report Number
    1416980-1996-09001
    Event Type
    Death
    Date Received
    June 12, 1996
    Date of Event
    April 22, 1996
    Report Date
    May 23, 1996
    Manufacturer
    BIOSEARCH MEDICAL PRODUCTS, INC.
    Product Code
    FPD
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    RPTR STATED THAT A PT EXPIRED AFTER A SECOND FEEDING TUBE WAS PLACED AND BEFORE AN X-RAY WAS TAKEN TO ESTABLISH THE LOCATION OF THE TUBE. THE FIRST FEEDING TUBE WAS REMOVED AFTER THE X-RAY SHOWED A BRONCHIAL LOCATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CLINTEC ENTERAL FEEDING TUBE FEEDING TUBE FPD BIOSEARCH MEDICAL PRODUCTS, INC. 9036

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Death