Recalls and Safety Alerts: Safety Information on Alaris SE Infusion Pumps
Published by Food and Drug Adminstration (FDA): Patient Safety October 31st, 2006 in Patient Safety, Regulatory AffairsCardinal Health, the owner of Alaris Products, has recalled all models of the Alaris Signature Edition (or SE) infusion pumps. These pumps have a design defect called “key bounce” that may cause over-infusion of medications. The affected models are…