BEUDAMED
    FDA Adverse Event Other Summary report: N

    ARROW

    MDR report key: 334893 · Received May 25, 2001

    Report

    Report Number
    334893
    Event Type
    Other
    Date Received
    May 25, 2001
    Date of Event
    January 31, 2001
    Report Date
    May 24, 2001
    Manufacturer
    ARROW INTERNATIONAL INC
    Product Code
    CAZ
    Report Source
    User Facility report
    Reporter Location
    NE, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DEVICE USED DURING PROCEDURE. WHEN EPIDURAL CATHETER WAS REMOVED, PART OF THE TIP REMAINED IN THE PT. TIP WAS NOT REMOVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    24536 ARROW EPIDURAL CATHETERIZATION KIT CAZ ARROW INTERNATIONAL INC SJ-05501 RF0121289

    Patients

    Seq Age Sex Outcome Treatment
    1 85 YR Other