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 ...

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 ...

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 ...

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 ...

For the fourth time already this month, the FDA has issued a notice formally bestowing a Class I label—denoting a heightened risk of serious injury or death—upon a recall of yet another drug delivery ...

LONDON--(BUSINESS WIRE)--The global smart syringe pumps market is expected to post a CAGR of nearly 9% during the forecast period 2019-2023, according to the latest market research report by Technavio ...

This tutorial discusses critical considerations requiring attention when designing an infusion pump, including FDA regulation, self-test circuitry, and meeting the IEC 60601-1 standard for electrical ...

Let us help you with your inquiries, brochures and pricing requirements Request A Quote Download PDF Copy Request A Quote Download PDF Copy Request A Quote Download ...

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 ...

Engineers working in the life sciences sector are facing increasing pressure to improve throughput and reduce total cost of ownership. Image Credit: Fluid Metering, Inc. Syringe pumps or inline piston ...

Dec 1 (Reuters) - The U.S. Food and Drug Administration (FDA) said on Friday that Becton Dickinson (BDX.N), opens new tab is recalling its Alaris infusion pumps due to compatibility issues with ...

The FDA is spotlighting a new medical device correction effort at Baxter over its large-volume Novum IQ infusion pump, following reports of 79 serious injuries and two deaths linked to potential under ...