The US Food and Drug Administration (FDA) has issued an early alert over a ‘potentially high-risk’ issue with certain Baxter Sigma Spectrum and Spectrum IQ infusion pumps. The agency’s ...
Baxter Healthcare has issued a recall for some Spectrum infusion pumps due to a potential defect involving missing motor mounting screws, which could lead to interruptions, delays or incorrect ...
The "North America and Europe Intravenous Infusion Pumps Market Size, Share & Trends Analysis Report by Product (Volumetric Infusion Pumps, Syringe Infusion Pumps), Disease Indication (Chemotherapy), ...
Manitoba's cancer authority has stopped using an infusion pump line — made by a company whose IV pumps ... Braun Infusomat primary lines and the current provincial contracted Baxter secondary lines," ...
The Sigma Spectrum and Spectrum IQ infusion systems. [Image courtesy of Baxter/FDA] The FDA today issued a notice warning of a potential high-risk issue with certain Baxter (NYSE:BAX) Spectrum ...
The Food and Drug Administration March 5 announced that Baxter Healthcare Corporation recalled its Spectrum infusion pumps due to the potential for missing motor mounting screws. The FDA said missing ...
Why it matters: While ICU benefitted from inflated IV solution sales in late 2024, Baxter's manufacturing ... ICU's other businesses—including its infusion pumps growing by 7% and consumables ...