ProductGuru Recalls

Brand

Datex-Ohmeda, Inc.: official recall notices

9 official recall or safety notices on this site name Datex-Ohmeda, Inc., dated between 2023-12-29 and 2026-07-30. They were issued by 1 authority: US FDA — Medical Devices (9).

Countries where the notices were issued: United States (9).

Name as written in the notices: Datex-Ohmeda, Inc.; Datex-Ohmeda Inc; DATEX--OHMEDA, INC.. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

YearNotices
20267
20241
20231

Notices by authority

AuthorityNotices
US FDA — Medical Devices9

All notices

DateAuthorityProductHazard (as classified)
2026-07-30US FDA — Medical DevicesAisys CS2 with Et Control, Datex-Ohmeda anesthesia system, Part Number 1011-9000-000—
2026-07-30US FDA — Medical DevicesEt Control, Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic—
2026-07-30US FDA — Medical DevicesAisys CS2, Datex-Ohmeda anesthesia system, Part Number 1011-9055-000—
2026-07-30US FDA — Medical DevicesAisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000—
2026-05-08US FDA — Medical DevicesGiraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator) Product identifiers: 20826—
2026-05-08US FDA — Medical DevicesGiraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with Integrated Resuscitation System (iRes) Pro—
2026-05-08US FDA — Medical DevicesPanda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-001 Impacted only if service blender M109—
2024-09-03US FDA — Medical DevicesGE Heathcare Giraffe OmniBed; neo natal incubator—
2023-12-29US FDA — Medical DevicesEVair 03 (Jun-air) air compressor, model numbers: 1609000 and 1609002—

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