BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    VANISHPOINT

    MDR report key: 16635028 · Received March 29, 2023

    Report

    Report Number
    16635028
    Event Type
    No answer provided
    Date Received
    March 29, 2023
    Date of Event
    March 13, 2023
    Report Date
    March 20, 2023
    Manufacturer
    RETRACTABLE TECHNOLOGIES, INC.
    Product Code
    MEG
    Report Source
    User Facility report
    Reporter Location
    MA
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    WHILE ADMINISTERING HEPARIN SUBCUTANEOUS TO A PATIENT THE NEEDLE FAILED, RETRACTED EARLY RESULTING IN HEPARIN SQUIRTING BACK AT ME AND LANDING IN MY EYE. I FLUSHED MY EYE WITH NO ILL EFFECT, BUT MY CONCERN IS THE NEEDLE FAILING. WHEN I DREW UP THE MEDICATION, I DID NOT DETECT ANY ISSUES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    954056 VANISHPOINT SYRINGE, ANTISTICK MEG RETRACTABLE TECHNOLOGIES, INC. G330A

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown