| Subject: | Acacia, Inc. Announces Worldwide Voluntary Recall of IV Extension Sets that use BD Q-Syte Luer Access Device |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 10 Feb 2010 - 12:00 pm |
| Acacia, Inc. (formally known as MPS Acacia) has voluntarily executed a product recall of certain lots of IV Extension Sets that contain the BD Q-Syte Luer Access Device. The BD Q-Syte Luer Access Device is a Needleless Valve manufactured by BD (Becton, Dickinson and Company) and was recently recalled. (See StayAlert notice published on February 9, 2010). Use of the affected BD Q-Syte Luer Access Device may cause an air embolism or leakage of blood and/or therapy, which may result in... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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