BEUDAMED
    FDA Enforcement Class II Terminated

    Eclipse Hypodermic Needle

    Recall: Z-1440-2017 · Reported March 22, 2017

    Enforcement

    Recall Number
    Z-1440-2017
    Event ID
    76129
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Becton Dickinson & Company
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    March 22, 2017
    Initiation Date
    December 20, 2016
    Classification Date
    March 10, 2017
    Termination Date
    April 20, 2018
    Address
    1 Becton Dr, N/A, Franklin Lakes, NJ, 07417-1815, United States

    Description

    Eclipse Hypodermic Needle

    Reason

    BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.

    Code Info

    N/A

    Distribution

    US Nationwide

    Quantity

    263 mm units