Please provide your email address to receive an email when new articles are posted on . The U.S. Food ad Drug Administration has issued a class 1 recall notice for model 35700 SIGMA Spectrum Infusion ...
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 ...
Baxter International Inc BAX has issued an urgent correction for its Spectrum V8 and Spectrum IQ infusion pumps, applicable in the U.S. and Puerto Rico, due to a ...
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 ...
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 ...
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 ...
November 15, 2010 — Sigma International General Medical Apparatus is voluntarily recalling its Spectrum model 35700 infusion pumps manufactured from October 2006 to March 2008 because of their ...
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