BEUDAMED
    FDA Adverse Event Other Summary report: N

    ARROW

    MDR report key: 748643 · Received July 6, 2005

    Report

    Report Number
    MW1035972
    Event Type
    Other
    Date Received
    July 6, 2005
    Date of Event
    July 1, 2005
    Report Date
    July 6, 2005
    Manufacturer
    ARROW INTERNATIONAL, INC.
    Product Code
    CAZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PATIENT WAS HAVING EPIDURAL CATHETER REMOVED BY ANESTHESIA PERSONNEL- PATIENT HAD KNEE REPLACEMENT. DURING REMOVAL CATHETER SNAPPED AND A PORTION OF AS YET UNK SIZE REMAINS IN PATIENT. DECISION WAS MADE NOT TO REMOVE; PT DISCHARGED HOME 3 DAYS LATER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARROW EPIDURAL CATHETERIZATION KIT CAZ ARROW INTERNATIONAL, INC. AM-05501 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR Other