FDA Recall
Terminated
Eclipse Hypodermic Needle
Recall: Z-1440-2017
·
Initiated December 20, 2016
Recall
- Recall Number
- Z-1440-2017
- Event Number
- 76129
- Firm
- Becton Dickinson & Company
- FEI Number
- 2243072
- Product Code
- FMI
- Status
- Terminated
- Root Cause
- Device Design
- Initiated
- December 20, 2016
- Terminated
- April 20, 2018
- Address
- 1 Becton Dr, Franklin Lakes, NJ, 07417-1815
Description
Eclipse Hypodermic Needle
Reason
BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.
Action
BD sent a Product Advisory Notice and Business Reply Card dated December 29, 2016 via UPS Ground delivery to their affected customers.
Distribution
US Nationwide
Quantity
263 mm units