FierceBiotech

FDA designates BD's wide-ranging Alaris infusion pump recall as Class I

BD is recalling hundreds of thousands of its Alaris infusion pumps and vital sign monitors due to multiple system faults, including software- and user-related issues. According to the FDA, the errors ...
Healio

FDA clears updated Alaris infusion pump; recall remediation remains ‘top priority’

Please provide your email address to receive an email when new articles are posted on . The FDA granted 510(k) clearance to Becton Dickinson’s updated Alaris infusion pump, allowing the company to ...
FierceBiotech

BD warns of 8 cybersecurity flaws in Alaris infusion pump systems

For BD, bad things seem to come in eights: The medtech giant issued a cybersecurity bulletin Thursday describing an octad of potential hacking risks it has discovered within certain versions of its ...
Seeking Alpha

BD expands recall of its Alaris Pump Module model 8100

The U.S. FDA said that BD (NYSE:BDX) has expanded its Class I voluntary recall to inform customers about the worst-case performance of the BD Alaris Pump Module model 8100 when used with certain ...
The Telegraph

Our Health: OSF HealthCare teams save lives by reporting fatal flaw in Alaris Pump Model 8100

PEORIA — On any given day, nurses provide compassionate, and, often, life-saving care to their patients. Sometimes that care can have a worldwide impact because of how health care — and those who work ...
Finanznachrichten

CareFusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall

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 units ...