⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Datex-Ohmeda recalls - full list & free alerts

7 official U.S. recalls involving Datex-Ohmeda in the last 12 months, most recently on 2026-09-23.

Check a lot code or UPC for Datex-Ohmeda · Recall guides

Get alerts for Datex-Ohmeda

Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.

Full list (7)

Datex-Ohmeda, Inc.: Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000
Medical DevicesFDA (device) · 2026-09-23 · Class II
Datex-Ohmeda, Inc.: Aisys CS2, Datex-Ohmeda anesthesia system, Part Number 1011-9055-000
Medical DevicesFDA (device) · 2026-09-23 · Class II
Datex-Ohmeda, Inc.: Aisys CS2 with Et Control, Datex-Ohmeda anesthesia system, Part Number 1011-9000-000
Medical DevicesFDA (device) · 2026-09-23 · Class II
Datex-Ohmeda, Inc.: Et Control, Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents, Field replac
Medical DevicesFDA (device) · 2026-09-23 · Class II
Datex-Ohmeda Inc: Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator) Product identifiers: 2082663-001, 2082663-002,
Medical DevicesFDA (device) · 2026-06-24 · Class I
Datex-Ohmeda Inc: Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with Integrated Resuscitation System (iRes) Product Identifiers: M1
Medical DevicesFDA (device) · 2026-06-24 · Class I
Datex-Ohmeda Inc: Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-001 Impacted only if service blender M1091607-R was installed
Medical DevicesFDA (device) · 2026-06-24 · Class I