Smiths Medical, a Minneapolis-based medical device-maker, is recalling its Medfusion syringe pumps after discovering a software issue that could cause the pumps’ low battery alarms to stop working.

FDA slaps Class 1 recall label on Minnesota-made syringe infusion pump The regulatory action affects more than 118,000 devices used in neonatal and pediatric patients, as well as adults in ICUs. The ...

Baxter International Inc. has scored FDA clearance for an infusion pump used to deliver small amounts of fluid at low rates, often in pediatric, neonatal and anesthesia care settings. The Novum Iq ...

Clinicians using programmable, or smart, syringe pumps should take precautions against mishaps that can occur at low infusion rates of high-risk, life-sustaining therapies, such as those at less than ...

Furthers Baxter’s continued innovation in medication delivery and management Integrates Baxter’s decades of leadership in infusion therapy with innovative digital health solutions to build on the ...

To date, there have been no reports of serious injury associated with this issue. Baxter International has issued an Urgent Medical Device Correction for the Novum IQ syringe infusion pump due to the ...