BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENTRIFLEX TUNGSTEN FEEDING TUBE

    MDR report key: 34900 · Received July 23, 1996

    Report

    Report Number
    34900
    Event Type
    Injury
    Date Received
    July 23, 1996
    Date of Event
    June 26, 1996
    Report Date
    July 19, 1996
    Manufacturer
    SHERWOOD MEDICAL CO.
    Product Code
    FPD
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    WI, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    NURSE ATTEMPTED INSERTION UNSUCCESSFULLY. ANESTHESIOLOGIST INSERTED W/O DIFFICULTY LATER. AIR AUSCULATED OVER UPPER RIGHT ABDOMEN. FOLLOW-UP SHOWED RIGHT LUNG HAD 50% PNEUMOTHORAX.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENTRIFLEX TUNGSTEN FEEDING TUBE FEEDING TUBE FPD SHERWOOD MEDICAL CO. 8 FR

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR Hospitalization