The FDA is spotlighting a new medical device correction effort at Baxter over its large-volume Novum IQ infusion pump, ...

Baxter (NYSE:BAX) is facing potential issues with its infusion pumps that has resulted in patient deaths, the FDA says.

The U.S. dominated the North American syringe infusion pumps market, supported by the high prevalence of chronic diseases and growing national healthcare expenditure.

With more than 325,000 pumps installed worldwide, the Plum A+ general purpose infusion system remains the proven choice for caregivers and clinicians alike.

Iradimed Corporation receives FDA clearance for MRidium® 3870 IV Infusion Pump, enhancing MRI-compatible fluid delivery technology.

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 ...

ICU Medical also received 510 (k) clearance for updated versions of the Plum Duo precision IV pump and LifeShield infusion safety software, completing the initial launch of the ICU Medical IV ...

ICU Medical also received 510 (k) clearance for updated versions of the Plum Duo precision IV pump and LifeShield™ infusion safety software, completing the initial launch of the ICU Medical IV ...