BEUDAMED
    FDA Adverse Event Summary report: N

    VANISHPOINT

    MDR report key: 3933992 · Received June 10, 2014

    Report

    Report Number
    3933992
    Date Received
    June 10, 2014
    Date of Event
    June 1, 2014
    Report Date
    June 10, 2014
    Manufacturer
    RETRACTABLE TECHNOLOGIES, INC.
    Product Code
    MEG
    Report Source
    User Facility report
    Reporter Location
    VA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    AFTER DRAWING UP THE PATIENT'S INSULIN, THE NURSE RECAPPED THE NEEDLE PRIOR TO THE INJECTION AND THE NEEDLE CAME OUT OF THE CAP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    337322 VANISHPOINT SYRINGE, ANTISTICK MEG RETRACTABLE TECHNOLOGIES, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *