BD Announces Worldwide Voluntary Recall ofBD Q-Syte[TM] Luer Access Devices and BD Nexiva[TM] Closed IV Catheter Systems

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: BD Announces Worldwide Voluntary Recall ofBD Q-Syte[TM] Luer Access Devices and BD Nexiva[TM] Closed IV Catheter Systems

BD Announces Worldwide Voluntary Recall ofBD Q-Syte[TM] Luer Access Devices and BD Nexiva[TM] Closed IV Catheter Systems
Tue, 09 Feb 2010 09:01:00 -0600

BD (Becton, Dickinson and Company) (NYSE:BDX) has voluntarily executed a product recall of certain lots ofBD Q-Syte™ Luer Access Devices and BD Nexiva™ Closed IV Catheter Systems. Use of the affected devices may cause an air embolism or leakage of blood and/or therapy, which may result in serious injury or death.

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