BD recall
This article was originally published in The Gray Sheet
Executive Summary
Becton Dickinson announces Feb. 8 the voluntary recall of BD-Q Syte luer access devices and BD Nexiva closed IV catheter systems used for infusion therapy. Damaged devices can cause embolism or leakage of blood or IV therapy fluids, resulting in injury or death. The Nexiva recall extends the scope of an earlier recall initiated Oct. 28, 2009, BD said