Datex-Ohmeda recalls Aespire 7100 anesthesia machines due to potential risk of patient limb circuit connection to the wrong gas outlet. All models 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 Aespire 7100 anesthesia machines that could cause patient injury if a breathing circuit limb is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port. Medical professionals using these machines should check their configuration to avoid this risk.
If a patient's breathing circuit limb is connected to the Auxiliary Common Gas Outlet (ACGO) port instead of the correct port, it could cause improper gas delivery and potentially harm the patient. This issue occurs because the machine's configuration allows for this mistake during setup.
Medical professionals who use Aespire 7100 anesthesia machines are most at risk. All devices with the Auxiliary Common Gas Outlet (ACGO) option are affected.
Check if your Aespire 7100 machine has the Auxiliary Common Gas Outlet (ACGO) option. All models with this configuration are affected, regardless of serial number or model number.
Verify if your Aespire 7100 machine has the Auxiliary Common Gas Outlet (ACGO) option by reviewing the machine's documentation or settings.
No, but you should check if your machine has the Auxiliary Common Gas Outlet (ACGO) option before use.
All Aespire 7100, 7100 (Variant), and 7100 S/5 Protiva models with the Auxiliary Common Gas Outlet (ACGO) option.
The recall does not specify a fix; users must check their configuration to avoid the risk.
We’ve drafted a message you can send Datex-Ohmeda to request your refund or repair — edit it as you like.
Subject: Recall Z-0074-2025 — Datex-Ohmeda Datex-Ohmeda Hello, I own a Datex-Ohmeda that is covered by recall Z-0074-2025 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.
