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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 ...
The recall notice stated that a specific lot of GE Healthcare Aisys and Avance machines control board ... are intended to provide general inhalation anesthesia and ventilation support to a wide ...
"The control board wiring harnesses have a defect which can cause the machine ... 1011-9000-000 and Avance model number 1009-9002-000. More information is available on the FDA's Web site. The ...
The U.S. Food and Drug Administration has issued a Class I recall of GE Healthcare’s Aisys and Avance Anesthesia systems ... which can cause the machine to unexpectedly shut down, terminating ...
The U.S. Food and Drug Administration has issued a Class I recall of GE Healthcare's Aisys and Avance Anesthesia systems ... which can cause the machine to unexpectedly shut down, terminating ...
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