News | News By Subject | News by Disease News By Date | Search News
Get Our FREE
Industry eNewsletter
email:    
   

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.

Read at News Release
Read at RTT News
Read at Nasdaq

comments powered by Disqus
   

ADD TO DEL.ICIO.US    ADD TO DIGG    ADD TO FURL    ADD TO STUMBLEUPON    ADD TO TECHNORATI FAVORITES