BEUDAMED
    FDA Adverse Event Other Summary report: N

    ENTRIFLEX FEEDING TUBE

    MDR report key: 3855816 · Received April 16, 2014

    Report

    Report Number
    9612030-2014-00021
    Event Type
    Other
    Date Received
    April 16, 2014
    Manufacturer
    COVIDIEN
    Product Code
    FPD
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    AN INVESTIGATION IS CURRENTLY UNDERWAY. UPON COMPLETION, THE RESULTS WILL BE FORWARDED.

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    233632 ENTRIFLEX FEEDING TUBE FEEDING TUBE FPD COVIDIEN

    Patients

    Seq Age Sex Outcome Treatment
    1