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 ...
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 ...
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 ...
CareFusion Alaris(R) Infusion System Recognized as One of the 'Best All-Around' Pumps In KLAS Report
SAN DIEGO, April 20 A new report from KLAS, an independent health care vendor research firm, concluded the CareFusion (NYSE: CFN) Alaris® System is one of the "best all-around" infusion pump options ...
CareFusion Corporation has initiated a class 1 recall of the Alaris PC unit model 8015 with software version 9.12 because of a voltage problem, according to the US Food and Drug Administration (FDA).
The Food and Drug Administration has assigned its most serious classification to the recall of 17,000 electronic infusion pumps made by CareFusion, saying a flaw in the devices could case serious ...
WellSpan Health and CareFusion, a BD company (NYSE: BDX), today announced the successful implementation of the Alaris ® System across all four WellSpan hospitals, with WellSpan York Hospital becoming ...
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 ...
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 ...
CareFusion has announced it has reached an agreement with Epic to make bi-directional connectivity available between CareFusion’s Alaris system and Epic’s electronic medical record platform, according ...
October 18, 2010 — A class 1 recall of CareFusion's Alaris point of care units (PC units), model 8015, has been issued, the US Food and Drug Administration (FDA) announced October 15. The device is a ...
(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.
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