BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VANISHPOINT SYRINGE

    MDR report key: 7295846 · Received February 23, 2018

    Report

    Report Number
    MW5075497
    Event Type
    Injury
    Date Received
    February 23, 2018
    Date of Event
    February 22, 2018
    Report Date
    February 22, 2018
    Manufacturer
    RETRACTABLE TECHNOLOGIES, INC.
    Product Code
    MEG
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PT USING VANISH POINT SYRINGE BY RETRACTABLE TECHNOLOGIES INC., LOT # A782A - NEEDLE BROKE OFF INTO LEFT DELTOID.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    137351 VANISHPOINT SYRINGE VANISHPOINT SYRINGE MEG RETRACTABLE TECHNOLOGIES, INC. A782A

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Required Intervention