BD Q-Syte Luer Access Devices: Recall
MedSun: Newsletter #46, March 2010

FDA MedWatch Safety Alert

BD, Acacia Inc. (known as MPS Acacia), and FDA notified healthcare professionals of the recall of certain lots of these devices. The BD Q-Syte Luer Access Device is a needleless valve manufactured by BD, intended for use with other infusion therapy products in the administration of fluids into the intravenous system. Use of the recalled devices may cause an air embolism or leakage of blood or therapeutic product which may result in serious injury or death.

Additional Information:

FDA MedWatch Safety Alert. BD Q-Syte Luer Access Devices: Recall. February 9, 2010.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm200137.htm


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