The Freedom60 Infusion Pump is designed to support dosing with 50 ml prefilled syringes, while the FreedomEDGE® Infusion System provides a compatible option for 20 mL prefilled syringe formats.

Fresenius has issued a software release to address issues that could interrupt treatment with its Ivenix large volume pumps.

Infusion pumps have been plagued with multiple FDA recalls in recent years, and some of the pumps identified in the recalls are still in use, according to a report by DotMed. For example, 200,000 ...

Pages Latest Report] According to a market research study published by Custom Market Insights, the demand analysis of Global ...

Please provide your email address to receive an email when new articles are posted on . The FDA announced a new initiative to address safety problems associated with external infusion pumps and is ...

You've probably seen an infusion pump, even though the name might make it sound like a mysterious piece of medical technology. These devices govern the flow of IV medications and fluids into patients.

Add Yahoo as a preferred source to see more of our stories on Google. By Jim Finkle BOSTON (Reuters) - The U.S. Food and Drug Administration on Friday advised hospitals not to use Hospira Inc's Symbiq ...

Renewed interest in hepatic arterial chemotherapy infusion pumps may be on the horizon, given promising overall survival findings in patients with advanced, unresectable cholangiocarcinoma. Dutch ...

A full week before the Food and Drug Administration issued an alert warning that Hospira’s Symbiq Infusion System smart pumps could be vulnerable to hackers, two BlackBerry officials were ...

Austin, Sept. 03, 2025 (GLOBE NEWSWIRE) -- Infusion Pump Market Size & Growth Analysis: According to a comprehensive report by SNS Insider, the Infusion Pump Market size was valued at USD 13.12 ...

In its second safety alert this year, Smiths Medical has issued a letter to its customers detailing a pair of potential issues with the infusion sets used alongside its CADD line of infusion systems.

The US Food and Drug Administration (FDA) has received reports of serious adverse events, including patient injury and death, associated with the use of implantable infusion pumps in the magnetic ...