BEUDAMED
    FDA Adverse Event Other Summary report: N

    ARROW

    MDR report key: 5367457 · Received June 20, 2005

    Report

    Report Number
    5367457
    Event Type
    Other
    Date Received
    June 20, 2005
    Date of Event
    June 6, 2005
    Report Date
    June 17, 2005
    Manufacturer
    ARROW INTERNATIONAL, INC.
    Product Code
    CAZ
    Report Source
    User Facility report
    Reporter Location
    MO, US
    Reporter Occupation
    2

    Narratives

    Description of Event or Problem · 1

    ((B)(4)). PT RECEIVED EPIDURAL WHICH WAS PLACED BY DR (B)(6). AFTER DELIVERY PT WAS PLACED IN PROPER POSITION TO REMOVE EPIDURAL CATHETER. MINIMAL RESISTANCE WAS MET WITH EPIDURAL CATH REMOVAL. EPIDURAL CATH WAS SLOWLY PULLING OUT, AND THEN SUDDENLY SNAPPED BACK. END OF CATHETER WAS NOTED TO BE FRAYED, TIP WAS NOT INTACT. DR. (B)(6) NOTIFIED OF EVENT, AND STATED THAT ANESTHESIA WOULD ASSESS PT IN THE AM. PT WAS NOTIFIED OF EVENT AND PLAN OF CARE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARROW ANESTHESIOLOGY PRODUCTS CAZ ARROW INTERNATIONAL, INC. HAVE POTENTIAL H'S

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR