BEUDAMED
    FDA Adverse Event Other Summary report: N

    BARD ACCESS SYSTEMS

    MDR report key: 842505 · Received April 17, 2007

    Report

    Report Number
    MW1042706
    Event Type
    Other
    Date Received
    April 17, 2007
    Date of Event
    April 12, 2007
    Report Date
    April 12, 2007
    Manufacturer
    C.R. BARD, BARD ACCESS SYSTEMS
    Product Code
    FMI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    RN REMOVING MEDIPORT HUBER NEEDLE FROM PT'S LEFT SUBCLAVIAN AREA. PATIENT EITHER MOVED OR JUMPED AND WHEN HE DID, RN'S LEFT INDEX FINGER WAS SCRAPED WITH THE HUBER NEEDLE. THE NEEDLE DID NOT CLOSE ON ITSELF AS IT ORDINARILY DOES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD ACCESS SYSTEMS HUBER NEEDLE FMI C.R. BARD, BARD ACCESS SYSTEMS * D628409

    Patients

    Seq Age Sex Outcome Treatment
    1 34 YR Other