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FDAFDA · Food and drugs·Recall number Z-1440-2017

Eclipse Hypodermic Needle

Published March 22, 2017 · Recall initiated: December 20, 2016

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Becton Dickinson & Company
Distributor
US Nationwide
Risk classification
Class II
Area (FDA)
device
Country
United States

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