The FDA labeled 22,769 Baxter drug infusion devices as a Class I recall after receiving reports of false upstream occlusion alarms, which can delay therapy. The two infusion pumps, SIGMA Spectrum ...

DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International Inc. (NYSE: BAX), a leader in innovative technology for medication delivery, today announced a new, comprehensive guide to building a smart ...

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 ...

For the third time in the last two years, Baxter has been hit with the FDA’s most serious label for a recall affecting its infusion pump systems. This time around, the Class I recall notice is linked ...

Hospira’s Lifecare PCA3 Drug Infusion pumps are susceptible to multiple remotely exploitable vulnerabilities that could not only brick the device but allow an attacker to run commands and put lives in ...

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 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 ...

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 ...

You've probably seen an infusion pump, even though the name might make it sound like a mysterious piece of medical technology. These devices govern the flow of IV medications and fluids into patients.

After a drawn-out approval process, medical equipment company Baxter International received regulatory clearance for a new infusion pump machine that is expected to help the company capture more of ...