BEUDAMED
    FDA Adverse Event Other Summary report: N

    FLEXTIP PLUS CATHETER

    MDR report key: 1277421 · Received January 2, 2009

    Report

    Report Number
    MW5009518
    Event Type
    Other
    Date Received
    January 2, 2009
    Date of Event
    December 12, 1980
    Report Date
    December 17, 2008
    Manufacturer
    ARROW INTERNATIONAL, INC
    Product Code
    BSO
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    UPON REMOVAL OF THE EPIDURAL CATHETER, THE TIP OF THE CATHETER WAS RETAINED IN THE PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLEXTIP PLUS CATHETER EPIDURAL CATHETER BSO ARROW INTERNATIONAL, INC

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR Other