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 ...
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 ...
ST. LOUIS (First Alert 4) - A local healthcare worker has a warning for patients at BJC facilities. If you need an IV for medicine or blood, one whistleblower tells First Alert 4 Investigates the ...
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 ...
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 ...
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 ...
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 ...
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