FDA Medical Device Recalls (openFDA)
Becton Dickinson Infusion Therapy: BD L-Cath EX (28ga x 20cm), L-Cath Catheter System
- Recall number
- Z-0785-04
- Recalling firm
- Becton Dickinson Infusion Therapy
- Product
- BD L-Cath EX (28ga x 20cm), L-Cath Catheter System
- Status
- Terminated
- Initiated
- 2004-03-09
- Posted
- 2004-07-20
- Terminated
- 2011-06-24
- Reason
- Catheters have stylets extending past the catheter tip, which, if not noticed could cause injury upon insertion.
- Root cause
- Other
- Action
- All consignees were notified by telephone on 03/09/2004, followed by a fax letter.
- Quantity
- 1850 units
- Distribution
- Nationwide. Foreign distribution to Australia, Canada and Japan.
- Lot, serial or model codes
- REF 384510, Lot Numbers 2158054, 2158055.
- 510(k) numbers
- ["K920755"]
- PMA numbers
- not on file
- Product code
- LJS
- 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