BEUDAMED
    FDA Adverse Event Other Summary report: N

    ENTRIFLEX

    MDR report key: 374020 · Received January 17, 2002

    Report

    Report Number
    MW1023903
    Event Type
    Other
    Date Received
    January 17, 2002
    Date of Event
    January 8, 2002
    Report Date
    January 8, 2002
    Manufacturer
    KENDALL
    Product Code
    FPD
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    FEEDING TUBE INSERTED BY PHYSICIAN PER PRODUCT INSTRUCTIONS, NO RESISTANCE MET. TUBE PERFORATED RIGHT LUNG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENTRIFLEX DUAL PORT FEEDING TUBE W/FLOW THROUGH STYLET FPD KENDALL 8884720858 U117203

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Other