Recall Z-0084-2025

Datex-Ohmeda, Inc. · initiated July 12, 2024

Class I Open, Classified

Class I – dangerous or defective products that could cause serious health problems or death

Product

Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under product names CONV KIT SCGO TO ACGO and ACGO ASSY FIELD INSTL. These kits are not affected specifically, however are included due to being purchased with or later used to convert to ACGO.

Codes / lots: No GTIN. Spare Part Numbers: 1009-8249-000, 1011-8071-000. Not model or lot specific. All devices of the indicated products configured with the AGCO option are potentially affected.

Reason for recall

Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

FDA-determined cause: Device Design

Action taken

GE Healthcare notified consignees on about 07/12/2024 via letter. Consignees were instructed to ensure all potential users complete the Preoperative Checkout procedure in its entirety, as detailed in the URM, make sure that the breathing circuit is correctly connected, only connect an auxiliary manual breathing circuit to the ACGO port, place the included addendum with the URM and inspect all potentially affected devices for the presence of covers applied to the ACGO Port and ACGO Switch. Additionally, customers were requested to complete and return the response form.

Details

Recall number
Z-0084-2025
Initiated
July 12, 2024
Posted by FDA
October 18, 2024
Product code
BSZ – Gas-Machine, Anesthesia
Quantity
649 units
Distribution
Worldwide distribution - US Nationwide and the countries of Aland Islands, ALBANIA, Algeria, Argentina, Australia, Austria, Azerbaijan, BAHAMAS, Bahrain, Bangladesh, BARBADOS, BELARUS, Belgium, Benin, Bermuda, Bolivia, BONAIRE, Bosnia and Herzegovina, Brazil, Brunei, Bulgaria, Cambodia, Cameroon, Canada, Chile, CHINA, Colombia, Costa Rica, Croatia, Curacao, Cyprus, Czech Republic, Denmark…
Recalling firm
Datex-Ohmeda, Inc., Madison, WI

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
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Z-0075-2025 Class IAespire 100. This anesthesia gas machine is intended to provide general inhalation…Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the… 07/12/2024Open, Classified
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Z-0077-2025 Class IAespire View. This anesthesia gas machine is intended to provide general inhalation…Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the… 07/12/2024Open, Classified
Z-0078-2025 Class IAvance. This anesthesia gas machine is intended to provide general inhalation anesthesia…Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the… 07/12/2024Open, Classified
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Z-0080-2025 Class IAvance CS2 and Avance CS2 Pro. These anesthesia gas machines are intended to provide…Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the… 07/12/2024Open, Classified
Z-0081-2025 Class IAisys. This anesthesia gas machine is intended to provide general inhalation anesthesia…Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the… 07/12/2024Open, Classified
Z-0082-2025 Class IAisys CS2. This anesthesia gas machine is intended to provide general inhalation…Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the… 07/12/2024Open, Classified
Z-0083-2025 Class IAisys CS2 with Et Control. This anesthesia gas machine is intended to provide general…Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the… 07/12/2024Open, Classified