CareFusion is recalling 7,418 units of its Alaris Syringe infusion pump, a corrective action that the FDA just deemed Class 1. This marks CareFusion's ninth Class 1 recall of an Alaris device since ...

FDA has assigned a Class I designation to a recall of CareFusion Alaris infusion pumps, originally announced last month. The agency gave the same designation to a recall of frame membranes that Elite ...

U.S. health regulators announced a recall of CareFusion's Alaris pump module Model 8100, saying a potential keypad malfunction in the infusion pump could cause serious injury or death. The U.S. Food ...

FDA has given Class I status to a Carefusion recall related to the Alaris Model 8100 infusion pump. A software failure in the pump had been identified in modules running software version 9.1.18. Last ...

CareFusion is recalling the PC unit of its Alaris infusion pump.--Courtesy of CareFusion CareFusion ($CFN) was plagued by regulatory problems all last summer, and now ...

CHICAGO, July 10 (Reuters) - Carefusion, the medical products business being spun off by Cardinal Health Inc , said it will resume shipments of its Alaris medication infusion pumps. Shipments had been ...

(Reuters) - Health regulators announced a recall of CareFusion's Alaris pump module Model 8100, saying a potential keypad malfunction in the infusion pump could cause serious injury or death. The U.S.