BEUDAMED
    FDA Adverse Event Injury Summary report: N

    B-D (BECTON DICKINSON & CO.)

    MDR report key: 217123 · Received March 31, 1999

    Report

    Report Number
    MW1016038
    Event Type
    Injury
    Date Received
    March 31, 1999
    Date of Event
    March 22, 1999
    Report Date
    March 22, 1999
    Manufacturer
    BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.
    Product Code
    FOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AK, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    NEEDLE INCORRECTLY INSERTED/LOCATED IN PROTECTIVE SHEATH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 B-D (BECTON DICKINSON & CO.) PRECISION GLIDE NEEDLE FOZ BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. 30 G1/2 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention