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 ...

The U.S. Food and Drug Administration (FDA) this week issued a Class I recall — its most serious — for the Medfusion syringe pump, the agency’s third major recall of the line of devices made in ...

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 ...

Smiths Medical, a Minneapolis-based medical device-maker, is recalling its Medfusion syringe pumps after discovering a software issue that could cause the pumps’ low battery alarms to stop working.

Smiths Medical has received FDA approval for a wireless version of its syringe infusion pump, according to a Smiths Medical news release. The new Medfusion 4000 wireless syringe infusion pump using ...

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 ...

ST. PAUL, Minn.--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its ...

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. Department of Homeland Security (DHS) recently issued a warning that Smiths Medical Medfusion 4000 wireless syringe infusion pumps contain a security vulnerability that can be exploited by ...

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 ...