FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: Eclipse Hypodermic Needle
- Recall number
- Z-1440-2017
- Recalling firm
- Becton Dickinson & Company
- Product
- Eclipse Hypodermic Needle
- Status
- Terminated
- Initiated
- 2016-12-20
- Posted
- not on file
- Terminated
- 2018-04-20
- Reason
- BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.
- Root cause
- Device Design
- Action
- BD sent a Product Advisory Notice and Business Reply Card dated December 29, 2016 via UPS Ground delivery to their affected customers.
- Quantity
- 263 mm units
- Distribution
- US Nationwide
- Lot, serial or model codes
- N/A
- 510(k) numbers
- ["K161170"]
- PMA numbers
- not on file
- Product code
- FMI
- Firm FEI
- 2243072
- Firm city
- Franklin Lakes
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28