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 ...
Becton, Dickinson and Company’s BDX, or popularly known as BD, initiated the recall of its infusion pumps last month after customer reports indicated software issues, potentially leading to inaccurate ...
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 ...
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 ...
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 ...
FRANKLIN LAKES, N.J., July 18, 2019 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today provided an update on two voluntary recalls ...
This story was originally published on MedTech Dive. To receive daily news and insights, subscribe to our free daily MedTech Dive newsletter. BD will pay a $175 million civil penalty to settle charges ...
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 ...
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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback