The U.S. Food and Drug Administration has issued a Class I recall of GE Healthcare’s Aisys and Avance Anesthesia systems, due to a defect in control board wiring harnesses, which can cause the machine ...
New York, June 22, 2021 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Anesthesia Machines Global Market Report 2021: COVID-19 Implications ...
The FDA slapped GE Healthcare's ($GE) recall of a number of ventilator and anesthesia machines with a Class I status--its most serious designation. GE itself ...
Officials have pointed to the anesthesia machines as a resource for hospitals. Anticipating ongoing shortages of ventilator machines as the coronavirus continues to spread across the country, states ...
May 13, 2010 — The US Food and Drug Administration (FDA) and General Electric (GE) have issued a class 1 recall of some lots of the GE Aisys and Avance anesthesia systems because of a control board ...
Please provide your email address to receive an email when new articles are posted on . The U.S. Food and Drug Administration has issued a Class I Medical Device Recall for GE Healthcare’s Aisys and ...
The US Food and Drug Administration (FDA) has approved the first software to semiautomate anesthesia delivery during surgery. The software, End-tidal (Et) Control, works with General Electric's (GE's) ...
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