Pioneering platform offers both large volume and syringe infusion pumps, is foundational for continued innovation in medication delivery and management Integrates Baxter's decades of leadership in ...

Baxter's preprogrammed infusion pump software recall lands FDA Class I label By Andrea Park Aug 13, 2021 10:15am Class I recall infusion pump medical device Software Platform ...

Vulnerabilities on battery units for medical infusion pump devices made by Baxter could allow for network access, DoS and man-in-the-middle attacks, highlighting IoT security issues and the need ...

CancerCare Manitoba has stopped the use of certain types of B. Braun infusion pump lines over concerns about leakage and chemotherapy drug spills. It comes after some models of Braun infusion ...

August 13, 2018 Our file Number: 18-109825-412 Scope Delivery accuracy testing requirements for infusion pumps to support new and amended medical device licence applications. Context This Notice ...

The now-recalled versions of both drug-dosing software programs were themselves originally meant to be a fix for Baxter’s last Class I infusion pump recall. In that case, the versions 8.01.00 ...

The U.S. Food and Drug Administration says infusion pumps have been linked to more than 56,000 injuries, deaths and malfunctions between 2005 and 2009.