Becton Dickinson & Company: Medical Device Recall in 2017 - (Recall #: Z-1440-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Eclipse Hypodermic Needle

Product Classification:

Class II

Date Initiated: December 20, 2016

Date Posted: March 22, 2017

Recall Number: Z-1440-2017

Event ID: 76129

Reason for Recall:

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

Status: Terminated

Product Quantity: 263 mm units

Code Information:

N/A

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated