Datex-Ohmeda recalls Aespire 7900 anesthesia machines due to risk of patient injury from incorrect circuit connections. All units with Auxiliary Common Gas Outlet (ACGO) option are affected.
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 all Aespire 7900 anesthesia machines that have the Auxiliary Common Gas Outlet (ACGO) option. This could cause serious harm if a patient's breathing circuit is mistakenly connected to the ACGO port during use.
If a patient's breathing circuit is accidentally connected to the Auxiliary Common Gas Outlet (ACGO) port instead of the correct port, it could cause improper gas delivery. This might lead to inadequate anesthesia or ventilation, potentially causing serious harm to the patient.
Medical professionals using the Aespire 7900 anesthesia machine with the ACGO option are most at risk. All units with this configuration are affected, regardless of serial number.
Check if your Aespire 7900 has the Auxiliary Common Gas Outlet (ACGO) option. All units with this configuration are affected, and no specific model or serial number is required.
Verify if your machine has the Auxiliary Common Gas Outlet (ACGO) option. This is the only configuration that is affected.
No, all Aespire 7900 units with the Auxiliary Common Gas Outlet (ACGO) option are affected. There are no specific model or serial numbers.
Incorrect connection could cause improper gas delivery, potentially leading to inadequate anesthesia or ventilation and serious patient harm.
No, but you should check if your machine has the ACGO option. If it does, you should verify connections before use to prevent potential harm.
We’ve drafted a message you can send Datex-Ohmeda to request your refund or repair — edit it as you like.
Subject: Recall Z-0076-2025 — Datex-Ohmeda Datex-Ohmeda Hello, I own a Datex-Ohmeda that is covered by recall Z-0076-2025 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.
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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.
