Becton Dickinson & Company recalls Eclipse Hypodermic Needle
- Recall date
- December 20, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1440-2017
- FDA classification
- Class II
- Brand / firm
- Becton Dickinson & Company
- Sold / distributed
- US Nationwide
Why it was recalled
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Eclipse Hypodermic Needle
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