BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENTRIFLEX

    MDR report key: 380480 · Received February 28, 2002

    Report

    Report Number
    MW1024277
    Event Type
    Injury
    Date Received
    February 28, 2002
    Date of Event
    February 18, 2002
    Report Date
    February 27, 2002
    Manufacturer
    SHERWOOD MEDICAL CO
    Product Code
    KNT
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PASSING FEEDING TUBE (ENTRIFLEX (BY: SHERWOOD DAVIS & GECK), PERFORATION OF PLEURAL TISSUE OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENTRIFLEX FEEDING TUBE KNT SHERWOOD MEDICAL CO * 131815

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention