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Terminated

Eclipse Hypodermic Needle

FDA Recall Z-1440-2017 · Posted None

Recalling FirmBecton Dickinson & Company
Recall StatusTerminated
Product CodeFMI
Date Initiated2016-12-20
Date Terminated2018-04-20
Product Quantity263 mm units

Reason for Recall

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

Firm Action

BD sent a Product Advisory Notice and Business Reply Card dated December 29, 2016 via UPS Ground delivery to their affected customers.

Root Cause

Device Design

Distribution Pattern

US Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K161170BD Eclipse Hypodermic NeedleBecton, Dickinson and Company · 2016-05-27

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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