FDA Medical Device Recalls (openFDA)
Becton Dickinson Infusion Therapy: BD Nexiva Closed IV Catheter System, 20 gauge
- Recall number
- Z-0585-05
- Recalling firm
- Becton Dickinson Infusion Therapy
- Product
- BD Nexiva Closed IV Catheter System, 20 gauge
- Status
- Terminated
- Initiated
- 2005-02-03
- Posted
- 2005-03-10
- Terminated
- 2005-05-17
- Reason
- The Y-luer connection may crack during normal product use.
- Root cause
- Other
- Action
- Customers were contacted by phone on 02/03/2005, and letters dated 02/10/05 were sent.
- Quantity
- 1560 catheters
- Distribution
- Domestic distribution: IL, UT, TX, FL. No foreign distribution. No distribution to military or VA facilities.
- Lot, serial or model codes
- Catalog Numbers: 383505, 383506, 383507 Lot Numbers: All lot numbers.
- 510(k) numbers
- ["K032843"]
- 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