FDA Medical Device Recalls (openFDA)
Becton Dickinson Infusion Therapy: BD First PICC 3F 65 cm Single Lumen Procedure Kit.
- Recall number
- Z-0832-03
- Recalling firm
- Becton Dickinson Infusion Therapy
- Product
- BD First PICC 3F 65 cm Single Lumen Procedure Kit.
- Status
- Terminated
- Initiated
- 2003-04-04
- Posted
- 2003-05-15
- Terminated
- 2003-07-30
- Reason
- A 4 Fr catheter was packaged in PICC convenience kits labeled as 3 Fr.
- Root cause
- Other
- Action
- All distributors and known hospitals were notified on 04/04/2003 by telephone, followed by a fax notification.
- Quantity
- 840 kits
- Distribution
- Nationwide
- Lot, serial or model codes
- Reference No. 384134, Lot No. 2326770.
- 510(k) numbers
- ["K945499"]
- 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