FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: BD 30ml Syringe Luer-Lok tip Sterile BD, Franklin Lakes, NJ Made in USA
- Recall number
- Z-0719-2007
- Recalling firm
- Becton Dickinson & Company
- Product
- BD 30ml Syringe Luer-Lok tip Sterile BD, Franklin Lakes, NJ Made in USA
- Status
- Terminated
- Initiated
- 2007-02-15
- Posted
- 2007-04-05
- Terminated
- 2007-07-19
- Reason
- The unit label on a limited number of syringes is incorrect, citing a 20 ml size. All other levels of labeling are correct, identifying the product as 30 ml size.
- Root cause
- Other
- Action
- Distributors were sent recall notification letters on February 1, 2007 Recall notification letters were sent to all direct accounts and potential end users via UPS second day air on February 15, 2007.
- Quantity
- 332,400 units
- Distribution
- Nationwide.
- Lot, serial or model codes
- Reorder number 309650 Lot numbers 6188613, 6188614
- 510(k) numbers
- ["K980987"]
- PMA numbers
- not on file
- Product code
- FMF
- 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