News

Fierce Healthcare14y
CareFusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall
On August 24, 2010, the company sent an urgent Medical Device Recall Notification to customers of its Alaris PC unit model 8015 stating that under certain wireless network conditions, affected ...
Medscape12y
Recall of Alaris Infusion Pump Computer Component
The US Food and Drug Administration (FDA) has notified healthcare providers of a class 1 recall of CareFusion's Alaris PC unit (model 8015) with software version 9.12. The Alaris PC unit is the ...
Medscape14y
Class 1 Recall of CareFusion's Infusion Pumps
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.
FierceBiotech12y
CareFusion endures another Class I pump recall
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 ...
Fox News12y
FDA recalls another CareFusion infusion pump | Fox News
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 ...
San Diego Union-Tribune14y
CareFusion pump recall gets FDA’s most serious classification
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 ...
FierceBiotech9y
CareFusion recalls its Alaris infusion pump, the franchise's 9th Class 1 recall since 2010 - Fierce Biotech
This marks CareFusion's ninth Class 1 recall of an Alaris device since 2010, ... Previous recalls have included other Alaris model numbers, including 8000 and 8015, ...
bdnews2414y
CareFusion recall classified as most serious type
On August 24, CareFusion recalled the Alaris PC model 8015 manufactured or serviced between December 2008 and September 2009. It said the pump could experience intermittent communication errors ...
Reuters12y
CORRECTED-CareFusion recalls another infusion pump | Reuters
Aug 22 (Reuters) - 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 ...
Finanznachrichten14y
CareFusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall - FinanzNachrichten.de
SAN DIEGO, Oct. 15 /PRNewswire/ -- CareFusion , a leading, global medical device company, issued the following update regarding its previously disclosed recall of approximately 17,000 Alaris® PC ...
Medindia14y
CareFusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall - Medindia
SAN DIEGO, Oct. 15 CareFusion (NYSE: CFN), a leading, global medical device company, issued the following update regarding its previously disclosed recall of approximately 17,000 Alaris® PC units ...