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Health Canada issued a Type II health-product recall for Carestation 850 anesthesia systems.
The systems can unexpectedly shut down when AC mains power is disconnected or lost.
The affected Carestation 850 model is 1012-9850-000, and healthcare users needing more information are advised to contact the manufacturer.
The recall involves the Carestation 850 anesthesia system.
Health Canada's recall notice identifies the affected model or catalogue number as 1012-9850-000.
The issue also concerns Carestation 850C anesthesia systems under the same reported shutdown condition.
According to Health Canada, the Carestation 850 and 850C anesthesia systems can experience an unexpected shutdown when AC mains power is disconnected or when AC mains power is lost.
The issue is classified as a medical-device performance problem.
Because anesthesia systems are used during medical procedures, reliable equipment performance is an important part of healthcare operations.
Health Canada has classified the action as a Type II health-product recall.
The recall classification indicates that the issue relates to a health product and requires attention from the relevant healthcare audience.
The official recall identifies the intended audience as healthcare.
Health Canada's notice lists:
The listed lot or serial number is not applicable in the recall notice.
The recall is directed toward the healthcare sector.
Facilities and healthcare professionals using the affected anesthesia systems should review the recall information and determine whether their equipment is included.
Healthcare organizations that require additional information about the recall are advised to contact the manufacturer.
Healthcare facilities using the affected Carestation systems should identify whether they have the recalled model.
They should review the official recall information and follow instructions provided by the manufacturer.
Health Canada specifically advises the healthcare audience to contact the manufacturer if additional information is required.
Anesthesia systems are used in medical settings where equipment performance is critical.
An unexpected shutdown can create an operational concern during a medical procedure, particularly when the equipment experiences a loss or disconnection of AC mains power.
The recall allows healthcare facilities to identify the affected equipment and obtain further information from the manufacturer.
The recall identifies Datex-Ohmeda, Inc. as the company associated with the affected product.
The company is based in Madison, Wisconsin, United States.
Health Canada published the recall as part of its health-product safety and recall system.
The recall date is listed as August 19, 2026.
Health Canada's notice was originally published on August 28, 2026, and the page was also updated on August 28.
The recall identification number is RA-82535.
This particular recall is directed toward the healthcare sector and concerns the performance of a medical device.
Health Canada's notice does not provide specific instructions for individual patients.
People who have questions about procedures involving the affected equipment should speak with their healthcare provider rather than making changes to their treatment on their own.
Medical-device recalls are used to alert healthcare organizations when a product has a potential safety, performance or quality issue.
In this case, Health Canada has identified an unexpected shutdown issue involving Carestation 850 and 850C anesthesia systems when AC mains power is disconnected or lost.
Healthcare facilities using the affected equipment can contact the manufacturer for additional information.
Health Canada has issued a Type II recall for Carestation 850 anesthesia systems because of an unexpected shutdown risk when AC mains power is disconnected or lost.
The affected Carestation 850 model is 1012-9850-000.
The recall is directed toward the healthcare sector, and facilities requiring additional information should contact the manufacturer.
Health Canada has issued a Type II recall for Carestation 850 anesthesia systems after identifying a risk of unexpected shutdown when AC mains power is disconnected or lost. The affected Carestation 850 model is 1012-9850-000.
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Health Canada has recalled the Carestation 850 anesthesia system and identified an issue affecting Carestation 850 and 850C systems.
The system can unexpectedly shut down when AC mains power is disconnected or AC mains power is lost.
Health Canada lists model or catalogue number 1012-9850-000 as the affected Carestation 850 product.
The product has been classified as a Type II health-product recall.
Health Canada advises healthcare users who require additional information to contact the manufacturer.
