Eclipse Hypodermic Needle
Reported: March 22, 2017 Initiated: December 20, 2016 #Z-1440-2017
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.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 263 mm units
- Distribution
- US Nationwide
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
Eclipse Hypodermic Needle. Recalled by Becton Dickinson & Company. Units affected: 263 mm units.
Why was this product recalled? ▼
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 22, 2017. Severity: Moderate. Recall number: Z-1440-2017.
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