BEUDAMED
    FDA Adverse Event Other Summary report: N

    ARROW FLEXITIP PLUS EPID CATHETER

    MDR report key: 41002 · Received August 30, 1996

    Report

    Report Number
    41002
    Event Type
    Other
    Date Received
    August 30, 1996
    Date of Event
    August 29, 1996
    Report Date
    August 30, 1996
    Manufacturer
    ARROW INTL, INC.
    Product Code
    BSO
    Report Source
    User Facility report
    Reporter Location
    VA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    AFTER C-SECTION, EPIDURAL CATHETER WAS REMOVED BY DR. A PORTION REMAINED IN PT'S BACK. (UNKNOWN AMOUNT) DR EXCISED SITE BUT UNABLE TO SEE REMAINDER OF CATHETER. X-RAY OBTAINED, STILL UNABLE TO SEE REMAINDER OF CATHETER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARROW FLEXITIP PLUS EPID CATHETER EPIDURAL CATHETER BSO ARROW INTL, INC. * SUSPECTED $192 6A

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Other