The Food and Drug Administration has categorized Smiths Medical’s correction of more than 50,000 syringe pumps in the U.S. as a Class I recall. Smiths Medical, which became part of ICU Medical in a $2 ...

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 (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 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 ...