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 ...
The Spectrum infusion pumps are used to deliver medications, nutrients and other fluids directly to a patient’s body via IV, so any interruptions to that delivery could be potentially life-threatening ...
Shares of Baxter International Inc. (BAX) upped nearly 1% following the disclosure of 510(k) clearance from the U.S. Food and Drug Administration (:FDA) for its next-generation SIGMA Spectrum Infusion ...
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 ...
In a safety warning first issued at the end of December 2021, Baxter identified a technical issue that may cause some of its Spectrum infusion pumps to fail to alert clinicians to repeated upstream ...
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) ...
DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International Inc. (NYSE: BAX), a leader in innovative technology for medication delivery, today announced the launch of DeviceVue, a comprehensive asset ...
Baxter International issued an urgent device correction Oct. 29 related to all of its Spectrum infusion pumps. The devicemaker said that deviations from specific cleaning methods may impair the pumps’ ...
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 ...
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 ...
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 ...