Z-0587-05

BD Nexiva Closed IV Catheter System, 24 gauge

Name: Z-0587-05 BD Nexiva Closed IV Catheter System, 24 gauge
Creator: Becton Dickinson Infusion Therapy
Published: 2005-02-03
License: https://open.fda.gov/license/

Becton Dickinson Infusion Therapy Systems Inc. / initiated 2005-02-03 / Terminated

FDA source

Becton Dickinson Infusion Therapy began a recall of BD Nexiva Closed IV Catheter System, 24 gauge on 2005-02-03. The reason FDA records is "The Y-luer connection may crack during normal product use". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0587-05
Status: Terminated
Initiated: 2005-02-03
Posted: 2005-03-10
Terminated: 2005-05-17
Recalling firm: Becton Dickinson Infusion Therapy Systems Inc.
Product: BD Nexiva Closed IV Catheter System, 24 gauge
Product code: FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Reason for recall: The Y-luer connection may crack during normal product use.
FDA root cause: Other
Action: Customers were contacted by phone on 02/03/2005, and letters dated 02/10/05 were sent.
Quantity in commerce: 1065 catheters
Distribution: Domestic distribution: IL, UT, TX, FL. No foreign distribution. No distribution to military or VA facilities.
Product codes and lots: Catalog Numbers: 383500, 383501 Lot Numbers: All lot numbers.

Product code FOZ

K032843Class IINexiva Closed IV Catheter SystemBecton Dickinson Infusion Therapy Systems, Inc. / cleared 2004-02-27

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)