BD Nexiva Closed IV Catheter System, 20 gauge
FDA device recall Z-0585-05 · posted 2005-03-10 · Terminated
Recall details
- Recalling firm
- Becton Dickinson Infusion Therapy
- Reason for recall
- The Y-luer connection may crack during normal product use.
- Action taken
- Customers were contacted by phone on 02/03/2005, and letters dated 02/10/05 were sent.
- Root cause
- Other
- Status
- Terminated
- Product code
- FOZ
- Quantity affected
- 1560 catheters
- Distribution
- Domestic distribution: IL, UT, TX, FL. No foreign distribution. No distribution to military or VA facilities.
- Date initiated
- 2005-02-03
- Date posted
- 2005-03-10
- Date terminated
- 2005-05-17
- Location
- Sandy, UT
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| NEXIVA CLOSED IV CATHETER SYSTEM (K032843) | Becton Dickinson Infusion Therapy Systems, Inc. | 2004-02-27 |