The U.S. Food ad Drug Administration has issued a class 1 recall notice for model 35700 SIGMA Spectrum Infusion Pump, due to the risk of sudden failure causing inaccurate flow conditions during use, ...
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 ...
DEERFIELD, Ill.--(BUSINESS WIRE)-- Baxter International Inc. (NYSE: BAX), a leader in innovative technology for medication delivery, today announced the U.S. Food and Drug Administration (FDA) ...
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 ...
June 15, 2012 — Sigma International General Medical Apparatus has expanded an earlier recall of its Spectrum model 35700 infusion pumps because of their tendency to fail suddenly without issuing an ...
The Spectrum IQ system also builds upon proven Spectrum infusion pump technology and Baxter’s comprehensive approach to patient safety to help make drug library compliance, protection for high-risk ...
Baxter International (NYSE:BAX) has issued an urgent medical device correction for software installed on certain Spectrum infusion pumps over concerns that they may be emitting false alarms that could ...
As predicted, not long after Baxter International issued an urgent safety communication about an issue with some of its Spectrum infusion pumps, it has been upgraded to a full-blown recall complete ...
The idea that medical devices can be hacked for nefarious purposes may sound like something out of movies, but as more and more devices provide connectivity, the risk is exponentially growing. In a ...
Though new software and other technologies can hugely improve safety and efficiency in healthcare by automating and preprogramming some of the most precise processes in a hospital, there are also ...
Baxter Healthcare Corp is recalling some models of its infusion pumps used to deliver medicine, blood and other fluids after it received over 3,500 reports of malfunctioning, the U.S. Food and Drug ...
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