BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CORFLO-ULTRA LIFE

    MDR report key: 33297 · Received March 13, 1996

    Report

    Report Number
    33297
    Event Type
    Malfunction
    Date Received
    March 13, 1996
    Date of Event
    January 22, 1996
    Report Date
    March 11, 1996
    Manufacturer
    CORPAK MEDSYSTEMS, INC.
    Product Code
    FPD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DEFECTIVE WIRE STYLET.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CORFLO-ULTRA LIFE ENTERAL FEEDING TUBE, 8FR, 43" FPD CORPAK MEDSYSTEMS, INC. A55KJ, A50KJ

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO