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Becton Dickinson & Company recalls Eclipse Hypodermic Needle
Recalled March 22, 2017 · FDA recall Z-1440-2017 · Becton Dickinson &
Hazard
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries. · FDA Class II
Units
263 mm units
Sold at
US Nationwide
Description
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.
Product
Eclipse Hypodermic Needle
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →