Eclipse Hypodermic Needle
FDA Recall #Z-1440-2017 — Class II — December 20, 2016
Product Description
Eclipse Hypodermic Needle
Reason for Recall
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.
Recalling Firm
Becton Dickinson & Company — Franklin Lakes, NJ
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
263 mm units
Distribution
US Nationwide
Code Information
N/A
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated