GE Healthcare has initiated a voluntary field corrective action for the Avance, Aisys and Avance CS anesthesia delivery systems with 8.00 (Avance and Aisys) or 10.00 (Avance CS) software due to a ...
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 ...
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 ...
Voluntary Field Corrective Action Issued for GE Healthcare's Avance, Aisys and Avance CS2 Anesthesia
MADISON, Wis.--(BUSINESS WIRE)-- GE Healthcare has initiated a voluntary field corrective action for the Avance, Aisys and Avance CS 2 anesthesia delivery systems with 8.00 (Avance and Aisys) or 10.00 ...
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 ...
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