FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: Microtainer Safety flow Lancets; Yellow Sterile Use once and discard; 2.2mm Blade Length; 1.0mm blade width; Becton Dickinson Vacutainer System; Becton Dickinson and Company; Franklin Lakes, NJ 07417
- Recall number
- Z-0045-2008
- Recalling firm
- Becton Dickinson & Company
- Product
- Microtainer Safety flow Lancets; Yellow Sterile Use once and discard; 2.2mm Blade Length; 1.0mm blade width; Becton Dickinson Vacutainer System; Becton Dickinson and Company; Franklin Lakes, NJ 07417
- Status
- Terminated
- Initiated
- 2007-09-26
- Posted
- 2007-10-18
- Terminated
- 2008-01-15
- Reason
- Potential for the blade and holder assembly to become loose and then separate from the main body of the lancet during the process of disposal.
- Root cause
- Process design
- Action
- Recall communication issued on or about 9/28/2007.
- Quantity
- 1,978,000 units
- Distribution
- Product distributed worldwide to Australia, Brazil, Canada, China, Colombia, Guatemala, Hong Kong, India, Indonesia, Mexico, Malaysia, New Zealand, Pakistan, Philippines, Singapore, Thailand, and United States.
- Lot, serial or model codes
- Catalog number 365759; Lot nuimbers: 2340323, 3017522, 3049342, 3069725, 3136072, 3149410, 3220675, 3213535, 2319394.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- F
- 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