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 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 ...

The U.S. Food and Drug Administration on Wednesday gave Minnesota-made syringe infusion pumps a Class 1 recall classification, the most serious category of market withdrawals. The device is made by ...

Citing eight product malfunctions, Smiths Medical has recalled more than 118,000 syringe infusion pumps after reports of one death and seven serious injuries. The Medfusion 3500 and 4000 pumps are ...

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 ...

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 ...

Smiths Medical has been urging healthcare providers to update tens of thousands of its hospital syringe pumps after identifying issues with outdated software, and now the FDA is helping to get the ...

Smiths Medical Inc., of Minneapolis, has undertaken a recall of its Medfusion 3500 and 4000 series of syringe infusion pumps because of software issues that could lead to over- or under-infusion of ...

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 ...

Smiths Medical can now bring wireless infusion pumps to U.S. hospitals. The FDA granted 510(k) clearance to the firm's Medfusion 4000 wireless syringe infusion pump with PharmGuard management software ...