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Terminated

BD Nexiva Closed IV Catheter System, 22 gauge

FDA Recall Z-0586-05 · Posted 2005-03-10

Recalling FirmBecton Dickinson Infusion Therapy
Recall StatusTerminated
Product CodeFOZ
Date Initiated2005-02-03
Date Terminated2005-05-17
Product Quantity660 catheters

Reason for Recall

The Y-luer connection may crack during normal product use.

Firm Action

Customers were contacted by phone on 02/03/2005, and letters dated 02/10/05 were sent.

Root Cause

Other

Distribution Pattern

Domestic distribution: IL, UT, TX, FL. No foreign distribution. No distribution to military or VA facilities.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K032843NEXIVA CLOSED IV CATHETER SYSTEMBecton Dickinson Infusion Therapy Systems, Inc. · 2004-02-27

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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