BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INTRODUCER NEEDLE, U-WING

    MDR report key: 285307 · Received July 6, 2000

    Report

    Report Number
    1710034-2000-00026
    Event Type
    Malfunction
    Date Received
    July 6, 2000
    Date of Event
    April 25, 2000
    Report Date
    July 3, 2000
    Manufacturer
    BD MEDICAL SYSTEMS
    Product Code
    FOZ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THREE ATTEMPTS MADE AFTER VEIN CANNULATED TO PASS 18 GAUGE CATHETER, UNABLE TO PASS THROUGH NEEDLE. PT EVENTUALLY TRANSFERRED TO RADIOLOGY FOR PICC PLACEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INTRODUCER NEEDLE, U-WING INTRAVASCULAR CATHETER FOZ BD MEDICAL SYSTEMS NA 911801

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other