Datex-Ohmeda recalls ACGO conversion kits that may cause patient breathing circuit errors if incorrectly connected. Affected kits include CONV KIT SCGO TO ACGO and ACGO ASSY FIELD INSTL. No specific model or lot numbers.
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 ACGO conversion kits that could lead to patient breathing circuit errors if incorrectly connected. This risk affects medical devices used in patient care settings.
If a patient's breathing circuit limb is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port, it could cause breathing circuit errors. This may lead to improper oxygen delivery or other patient safety issues.
Healthcare providers using these kits for medical equipment conversions are most at risk. Patients using the equipment with improper connections could face breathing circuit errors.
Check for kits labeled CONV KIT SCGO TO ACGO or ACGO ASSY FIELD INSTL. These kits are used with medical devices configured for the ACGO option and were sold without specific model or lot numbers.
Look for labels indicating CONV KIT SCGO TO ACGO or ACGO ASSY FIELD INSTL on the kit packaging.
Ensure your medical device is configured with the ACGO option before using the kit.
The risk is that if a patient's breathing circuit limb is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port, it could cause breathing circuit errors.
No, the kits are not model or lot specific. All devices configured with the ACGO option are potentially affected.
Check for labels CONV KIT SCGO TO ACGO or ACGO ASSY FIELD INSTL on the kit packaging.
We’ve drafted a message you can send Datex-Ohmeda to request your refund or repair — edit it as you like.
Subject: Recall Z-0084-2025 — Datex-Ohmeda Datex-Ohmeda Hello, I own a Datex-Ohmeda that is covered by recall Z-0084-2025 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.
