Datex-Ohmeda, Inc.

Frequent Recalls

7

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-06-24 to 2026-09-23

Date	Source	Product	Brand	Severity	Units
2026-09-23	FDA Device	FDA Recall: Aisys CS2 with Et Control, Datex-Ohmeda anesthesia system, Part Number 1011-9000-000	Datex-Ohmeda, Inc.	Class II	N/A
2026-09-23	FDA Device	FDA Recall: Et Control, Software option for anesthesia gas machine to achieve and maintain targeted end tidal ox	Datex-Ohmeda, Inc.	Class II	N/A
2026-09-23	FDA Device	FDA Recall: Aisys CS2, Datex-Ohmeda anesthesia system, Part Number 1011-9055-000	Datex-Ohmeda, Inc.	Class II	N/A
2026-09-23	FDA Device	FDA Recall: Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000	Datex-Ohmeda, Inc.	Class II	N/A
2026-06-24	FDA Device	FDA Recall: Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with Integrated Resuscitati	Datex-Ohmeda Inc	Class I	N/A
2026-06-24	FDA Device	FDA Recall: Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-001 Impacted only if	Datex-Ohmeda Inc	Class I	N/A
2026-06-24	FDA Device	FDA Recall: Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator) Produc	Datex-Ohmeda Inc	Class I	N/A

Datex-Ohmeda, Inc. Recalls | WatchRecall