| Subject: | Worldwide Voluntary Recall of Becton, Dickinson and Company’s BD Q-Syte Luer Access Devices and BD Nexiva Closed IV Catheter Systems |
| Category: | Food and Drug Administration (FDA)
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| Published: | Tue, 9 Feb 2010 - 01:00 pm |
| BD (Becton, Dickinson and Company) has voluntarily executed a product recall of certain lots of BD 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. Please see the recall notice, a link is provided below, for recalled product lot numbers. The approximately 2.8 million BD Q-Syte and 2.9 million BD Nexiva units containing 5 million BD... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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