Please provide your email address to receive an email when new articles are posted on . Automated syringe pump induction may be associated with less propofol waste after IV anesthesia vs. manual ...

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 ...

Smiths Medical notified customers of 50,743 syringe pumps of a software issue that can cause serious injury or death, the FDA said Feb. 14. An earlier software version of the product, the Medfusion ...

Nov 20 (Reuters) - The U.S. Food and Drug Administration on Monday warned healthcare providers and facilities not to use Cardinal Health's (CAH.N), opens new tab Monoject syringes with ...

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 ...

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 ...

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Just a week after issuing a notice giving its most serious rating to Cardinal Health’s recall of certain syringes, the FDA has put out a letter to healthcare providers warning that the recall may not ...

Smiths Medical has warned customers of more than 135,000 Medfusion syringe pumps about problems associated with earlier software versions. On March 5, the FDA posted an alert for 85,961 Medfusion ...