FDA Medical Device Recalls (openFDA)
Becton Dickinson Medical Systems: BD DTX Plus, Custom dual-line pressure monitoring kit.
- Recall number
- Z-1565-05
- Recalling firm
- Becton Dickinson Medical Systems
- Product
- BD DTX Plus, Custom dual-line pressure monitoring kit.
- Status
- Terminated
- Initiated
- 2005-07-01
- Posted
- 2005-09-21
- Terminated
- 2011-08-09
- Reason
- Actuating tab may detach from the stopcock body, allowing fluid leak.
- Root cause
- Other
- Action
- Consignees were notified by phone and fax on 07/01/2004.
- Quantity
- 405 units
- Distribution
- Nationwide, including VA facilities in NY, SD, IL, OH and military facilities in GA, NC and Guam. Foreign distribution to Japan.
- Lot, serial or model codes
- Part number 687341, Lot Numbers: 410177, 411063, 411540.
- 510(k) numbers
- ["K935782"]
- PMA numbers
- not on file
- Product code
- DXN
- 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