Datex-Ohmeda recalls Aespire 100 anesthesia machines due to potential risk of patient injury from incorrect breathing circuit connections. Medical professionals should follow official instructions for safe use.
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 100 anesthesia machines because a mistake in connecting patient breathing circuits could cause harm. This is a serious risk for medical professionals using the equipment during surgery.
If a patient's breathing circuit is incorrectly connected to the Auxiliary Common Gas Outlet (ACGO) port, it could cause improper gas delivery. This might lead to inadequate anesthesia or oxygen levels, potentially harming the patient.
Medical professionals who use the Aespire 100 anesthesia machines for patient care are most at risk. Patients receiving anesthesia through this equipment could be affected if the connection error occurs.
The Aespire 100 anesthesia machine is made by Datex-Ohmeda Inc. It was sold with GTIN 00840682102261. Medical professionals using this equipment for anesthesia procedures are likely affected.
Verify that patient breathing circuits are correctly connected to the main gas port, not the Auxiliary Common Gas Outlet (ACGO) port.
The recall is for medical professionals using the equipment. Patients are not directly affected unless the connection error occurs during anesthesia.
The Aespire 100 anesthesia machine from Datex-Ohmeda Inc with GTIN 00840682102261 is recalled. Medical professionals using this equipment for anesthesia procedures are likely affected.
The official recall does not specify a remedy. Medical professionals should check connection setup to avoid incorrect circuit connections.
We’ve drafted a message you can send Datex-... to request your refund or repair — edit it as you like.
Subject: Recall Z-0075-2025 — Datex-... Datex-... Hello, I own a Datex-... that is covered by recall Z-0075-2025 from Datex-.... 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.
