FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder.
- Recall number
- Z-0372-06
- Recalling firm
- Becton Dickinson & Company
- Product
- BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder.
- Status
- Terminated
- Initiated
- 2005-12-01
- Posted
- 2006-01-11
- Terminated
- 2007-04-30
- Reason
- Cracked finger grip luer adapter components on the Push Button Blood Collection Set.
- Root cause
- Other
- Action
- Recall notification was sent out to the customers on 12/5/2005.
- Quantity
- 118200 each
- Distribution
- The device was shipped to 23 wholesalers, 5 hospitals, and 1 VA govt. account nationwide.
- Lot, serial or model codes
- Catalog # -- Lot #: 367352 -- 5188576; 367352 -- 5208448; 367352 -- 5217290; 368656 -- 5164491; 368656 -- 5164526; 368656 -- 5187894; 368656 -- 5192496; 368656 -- 5220204; 368656 -- 5238936.
- 510(k) numbers
- ["K011984"]
- PMA numbers
- not on file
- Product code
- KSR
- 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