FDA Classifies Recall of a Component of CareFusion Corporation's Alaris Infusion Pump as Class I  
8/2/2012 8:22:06 AM

The U.S. Food and Drug Administration classified the recall of the PC unit of a certain model of the CareFusion Alaris Infusion pump as Class I on Wednesday. The Alaris PC unit model 8015 has a component that is causing error messages like “System Error” or “Missing Battery Error” at startup. On June 27, CareFusion(NYSE:CFN) sent a recall notification asking users to stop using the unit if either of the error messages were seen.