New devices address infusion delivery variability and expand the ICU Medical IV Performance Platform. Unlike traditional pumps that rely on specific setups and conditions for accurate delivery, ...

A recall of nearly 62,800 replacement batteries used in several of ICU Medical’s infusion pumps has received the FDA’s Class I rating—the agency’s most serious, denoting a higher risk of serious ...

ICU Medical receives FDA clearance for Plum Duo infusion pump and LifeShield infusion safety software, part of the new ICU Medical IV performance platform ICU Medical Inc. wants hospitals to question ...

With roots as a supplier of infusion consumables, ICU enhanced its product mix through the transformative acquisition of Hospira Infusion Systems from Pfizer in 2017 by bringing infusion pumps, a ...

KLAS Research recognizes Plum 360 as 2021 Best in KLAS for Smart Pump EMR-Integrated, highlighting ICU Medical's pioneering efforts to advance industry standards for smart infusion pump ...

The U.S. FDA’s April 4, 2025, warning letter to ICU Medical Inc. cited the company for failure to file a new 510(k) for changes to software used in an infusion pump, but those changes may have been ...

Medical device maker ICU Medical changed the designs of infusion pumps made in Minnesota without properly clearing important regulatory checks after a recent recall, according to a Food and Drug ...

Shares of ICU Medical (NASDAQ:ICUI) spiked on Friday after Piper Sandler initiated its coverage with an Overweight rating and a $145 price target, citing an imminent new product cycle wave for the ...

Smiths Medical, an entity of ICU Medical, is recalling more than 108,000 syringe pumps because a false alarm may sound. The recall includes 108,816 Medfusion Syringe Pumps that were distributed across ...

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 ...