BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENTERAL FEEDING TUBE WITH STYLET

    MDR report key: 4387490 · Received December 30, 2014

    Report

    Report Number
    MW5039968
    Event Type
    Injury
    Date Received
    December 30, 2014
    Date of Event
    April 27, 2014
    Report Date
    April 27, 2014
    Manufacturer
    CORPAK MEDSYSTEMS, INC.
    Product Code
    FPD
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NM, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    DOBHOFF FEEDING TUBE WAS INSERTED IN A PATIENT WITH AN ALREADY TENUOUS RESPIRATORY SYSTEM, BORDERING ON REINTUBATION. CHEST X-RAY REVEALED THE DOBHOFF TUBE TO BE IN THE LEFT LUNG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    858314 ENTERAL FEEDING TUBE WITH STYLET ENTERAL FEEDING TUBE WITH STYLET FPD CORPAK MEDSYSTEMS, INC. CORFLO-ULTRA LIT 8FR. 66215

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Required Intervention