On April 20, 2022, Rapid7 discovered vulnerabilities in two TCP/IP–enabled medical devices produced by Baxter Healthcare. The flaws, four in total, affected the company’s SIGMA Spectrum Infusion Pump ...

Baxter recalled over 277,000 infusion pumps due to the risk of the device failing to alarm users of repeated upstream occlusion events. The SIGMA Spectrum Infusion Pump with Master Drug Library ...

DEERFIELD, Ill., & SALT LAKE CITY--(BUSINESS WIRE)-- Intermountain Healthcare and Baxter Healthcare Corporation today announced the successful integration of the SIGMA Spectrum Infusion System into ...

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 notice ...

Baxter International Inc. announced at the ASHP 2016 meeting the launch of the Sigma Spectrum Safety Management System, which adds features designed to help minimize infusion programming risks. The ...

For the third time in the last two years, Baxter has been hit with the FDA’s most serious label for a recall affecting its infusion pump systems. This time around, the Class I recall notice is linked ...

DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International (NYSE: BAX) this week announced the results of a retrospective analysis of data from Sigma Spectrum Infusion System pumps that found 90 percent ...

Baxter International says the suspension of shipments of certain products led to its decision to eliminate 91 positions at its Medina plant. The Illinois-based health care products company said 370 ...

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 dosing ...