FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950.
- Recall number
- Z-1525-06
- Recalling firm
- Becton Dickinson & Company
- Product
- BD 1mL SafetyGlide Allergy and Tuberculin Syringes. Reorder Number 305945 and 305950.
- Status
- Terminated
- Initiated
- 2006-07-24
- Posted
- 2006-09-28
- Terminated
- 2007-12-03
- Reason
- BD received reports of needle assembly disengagement from the syringe.
- Root cause
- Other
- Action
- Recall letters were sent to all wholesalers and end users on 7/28/2006.
- Quantity
- 1,294,200 units
- Distribution
- Nationwide.
- Lot, serial or model codes
- Reorder Number: 305945 Lot: 5312395 and 5312394. Reorder Number: 305950 Lot: 5319508 and 5300175.
- 510(k) numbers
- ["K992734"]
- PMA numbers
- not on file
- Product code
- MEG
- 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