BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    BD PRECISIONGLIDE

    MDR report key: 13633856 · Received March 1, 2022

    Report

    Report Number
    13633856
    Event Type
    No answer provided
    Date Received
    March 1, 2022
    Date of Event
    February 7, 2022
    Report Date
    February 10, 2022
    Manufacturer
    BECTON, DICKINSON AND COMPANY
    Product Code
    FMI
    Report Source
    User Facility report
    Reporter Location
    CT
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    NO PATIENT INVOLVEMENT. PHARMACY TECHNICIAN WAS ABOUT TO PREPARE MEDICATION AND NOTICED DEBRIS AT HUB OF NEEDLE. PICTURES TAKEN AND SHARED WITH MANUFACTURER. SYSTEM WIDE SBAR SENT OUT FOR AWARENESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1793976 BD PRECISIONGLIDE NEEDLE, HYPODERMIC, SINGLE LUMEN FMI BECTON, DICKINSON AND COMPANY 1210583

    Patients

    Seq Age Sex Outcome Treatment
    1 0 DA Unknown