Type 1 diabetes is more prevalent in Finland than anywhere else in the world, affecting approximately 50,000 people. New ...

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.

Smiths Medical has recalled ambulatory infusion pumps to address three problems that pose safety risks.

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 ...