BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GRINER NEEDLE

    MDR report key: 17690972 · Received September 5, 2023

    Report

    Report Number
    MW5145181
    Event Type
    Malfunction
    Date Received
    September 5, 2023
    Date of Event
    August 25, 2023
    Report Date
    August 29, 2023
    Manufacturer
    GREINER BIO-ONE NORTH AMERICA, INC.
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    501
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    WHEN LAB TECH FINISHED DRAWING BLOOD AND RETRACTED THE NEEDLE BLOOD SHOT ON PATIENT CLOTHES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1379224 GRINER NEEDLE NEEDLE, HYPODERMIC, SINGLE LUMEN FMI GREINER BIO-ONE NORTH AMERICA, INC. G21093BF

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown