FDA Medical Device Recalls (openFDA)
Becton Dickinson Infusion Therapy: Careflow 7Fr x 20cm 3-lumen Central Venous Catheter Tray
- Recall number
- Z-0630-05
- Recalling firm
- Becton Dickinson Infusion Therapy
- Product
- Careflow 7Fr x 20cm 3-lumen Central Venous Catheter Tray
- Status
- Terminated
- Initiated
- 2005-01-10
- Posted
- 2005-03-18
- Terminated
- 2005-04-12
- Reason
- Various procedure trays and kits may have an insufficient seal, thus compromising sterility.
- Root cause
- Other
- Action
- Customers were contacted by telephone and by letters dated 01/10/05.
- Quantity
- 5 units
- Distribution
- Domestic distribution: WI. International distribution: Puerto Rico, Virgin Islands. There were no military or VA facilities.
- Lot, serial or model codes
- Ref. No. 681725, Lot No. 405622
- 510(k) numbers
- ["K033500"]
- PMA numbers
- not on file
- Product code
- FOZ
- Firm FEI
- 1710034
- Firm city
- Sandy
- Firm state
- UT
- 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