ST. PAUL, Minn.--(BUSINESS WIRE)-- Smiths Medical, a leading global medical device manufacturer, announced today it received a license from Health Canada and launched its Medfusion ® 4000 syringe ...

Smiths Medical has warned customers of more than 135,000 Medfusion syringe pumps about problems associated with earlier software versions. On March 5, the FDA posted an alert for 85,961 Medfusion ...

The Food and Drug Administration has classified a recall of about 600 pediatric drug-infusion pumps made by Plymouth-based Smiths Medical as a Class 1 recall, meaning that a software problem in the ...

The US Department of Homeland Security (DHS) has warned of eight new vulnerabilities in several popular syringe infusion pump models which could allow a remote hacker to alter how they work. An ...

US government issues security warnings for hospital syringe pumps susceptible to hacking The U.S. Department of Homeland Security issued a warning Sept. 7 notifying health facilities of potential ...

A syringe pump made by a Minneapolis-based company is being recalled for risks that could cause life-threatening injuries or death. The Food and Drug Administration (FDA) issued a Class I correction ...

The U.S. Food and Drug Administration issued a Class I recall, the agency's most serious, for the Medfusion syringe pump, the third major FDA recall for the line of devices made in Oakdale. Smiths ...

MINNEAPOLIS--(BUSINESS WIRE)--Smiths Medical has become aware of an issue where certain Medfusion ® 3500 and 4000 syringe pumps with firmware versions listed below may not operate as expected. Due to ...

The last place you should have to worry about being hacked is laid out in a hospital bed. But as wireless devices continue to fill patient rooms, those fears can’t help but grow. Last week, the ...

ST. PAUL, Minn.--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it received a license from Health Canada and launched its Medfusion ® 4000 syringe ...