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Recall Observatory FDA recall evidence

Device product

Eclipse Hypodermic Needle

Z-1440-2017

December 20, 2016

Class II

Product summary

Firm
Becton Dickinson & Company
Event
Event 76129
Status
Terminated
Classification
Class II
Quantity
263 mm units
Official record key
device-enforcement:Z-1440-2017

Official wording

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

Code information: N/A

Distribution pattern: US Nationwide

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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