Datex-Ohmeda recalls Avance CS2 and CS2 Pro anesthesia machines due to potential risk of connecting patient breathing circuits to the wrong gas outlet, which could cause unsafe anesthesia delivery.
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Datex-Ohmeda is recalling Avance CS2 and CS2 Pro anesthesia machines because a patient breathing circuit might be mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port. This could lead to unsafe anesthesia delivery during medical procedures.
If a patient's breathing circuit is accidentally connected to the Auxiliary Common Gas Outlet (ACGO) port instead of the correct port, it could deliver the wrong type of anesthesia gas. This might cause unsafe anesthesia levels or inadequate ventilation during surgery.
Medical professionals using these anesthesia machines are most at risk. Patients receiving anesthesia through these devices could be affected if the breathing circuit is incorrectly connected.
Check for model numbers 1009-9050-000, 1011-9050-000, 1009-9002-000, or 1009-9212-000 on the device. All serial numbers are affected if the device has the AGCO option configured.
Verify that the patient's breathing circuit is connected to the correct port, not the Auxiliary Common Gas Outlet (ACGO) port.
The recall is due to a potential risk that a patient's breathing circuit might be mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port, which could lead to unsafe anesthesia delivery.
Devices with model numbers 1009-9050-000, 1011-9050-000, 1009-9002-000, or 1009-9212-000 and the AGCO option configured are affected. All serial numbers are included.
No, but you should check that the breathing circuit is connected to the correct port to avoid potential unsafe anesthesia delivery.
We’ve drafted a message you can send Datex-Ohmeda to request your refund or repair — edit it as you like.
Subject: Recall Z-0080-2025 — Datex-Ohmeda Datex-Ohmeda Hello, I own a Datex-Ohmeda that is covered by recall Z-0080-2025 from Datex-Ohmeda. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
