Datex-Ohmeda recalls

Datex-Ohmeda has 30 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 23 Sep 2026. 26 are still ongoing. 7 were reported in the last 12 months.

Total recalls30since 2018
Last 12 months7reported
Class I2170% of total
Ongoing26latest 23 Sep 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 21 70%Class II 9 30%Class III 0 0%

Why datex-ohmeda is recalled

By year

Ongoing datex-ohmeda recalls

26 active

All datex-ohmeda recalls, newest first

30 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIAisys, Datex-Ohmeda anesthesia system recalledDatex-OhmedaDevice MalfunctionNationwide
DeviceCLASS IIAisys CS2, Datex-Ohmeda anesthesia system recalledDatex-OhmedaDevice MalfunctionNationwide
DeviceCLASS IIEt Control recalled by Datex-OhmedaDatex-OhmedaDevice MalfunctionNationwide
DeviceCLASS IIAisys CS2 with Et Control, Datex-Ohmeda anesthesia system recalledDatex-OhmedaDevice MalfunctionNationwide
DeviceCLASS IPanda Freestanding Warmer, Infant Radiant Warmer Product recalledDatex-OhmedaDevice MalfunctionWI
DeviceCLASS IGiraffe Warmer with Integrated Resuscitation System (iRes) recalledDatex-OhmedaDevice MalfunctionWI
DeviceCLASS IGiraffe Stand-alone Infant Resuscitation System recalled by Datex-OhmedaDatex-OhmedaDevice MalfunctionWI
DeviceCLASS IGE Healthcare Giraffe Omnibed Carestation CS1 recalled by Datex--ohmedaDatex--ohmedaDevice MalfunctionWI
DeviceCLASS IGE Healthcare Giraffe Incubator Carestation CS1, Infant Incubator recalledDatex--ohmedaDevice MalfunctionWI
DeviceCLASS IAespire View recalled by Datex-OhmedaDatex-OhmedaOtherNationwide
DeviceCLASS IAuxiliary Common Gas Outlet recalled by Datex-OhmedaDatex-OhmedaOtherNationwide
DeviceCLASS IAespire 7900. This anesthesia gas machine is intended to provide recalledDatex-OhmedaOtherNationwide
DeviceCLASS IAmingo. OUS only recalled by Datex-OhmedaDatex-OhmedaOtherNationwide
DeviceCLASS IAvance. This anesthesia gas machine is intended to provide recalledDatex-OhmedaOtherNationwide
DeviceCLASS IAespire 7100, 7100 (Variant) recalled by Datex-OhmedaDatex-OhmedaOtherNationwide
DeviceCLASS IAisys. This anesthesia gas machine is intended to provide recalledDatex-OhmedaOtherNationwide
DeviceCLASS IAisys CS2. This anesthesia gas machine is intended recalledDatex-OhmedaOtherNationwide
DeviceCLASS IAvance CS2 and Avance CS2 Pro recalled by Datex-OhmedaDatex-OhmedaOtherNationwide
DeviceCLASS IAespire 100. This anesthesia gas machine is intended recalledDatex-OhmedaOtherNationwide
DeviceCLASS IAisys CS2 with Et Control recalled by Datex-OhmedaDatex-OhmedaOtherNationwide
DeviceCLASS IGE Heathcare Giraffe OmniBed Carestation recalled by Datex--ohmedaDatex--ohmedaDevice MalfunctionWI
DeviceCLASS IGE Heathcare Giraffe OmniBed recalled by Datex--ohmedaDatex--ohmedaDevice MalfunctionWI
DeviceCLASS IEVair air compressor recalled by Datex-OhmedaDatex-OhmedaTemperature AbuseWI
DeviceCLASS IEvAir Cprsr Kit Upgrade: a) Diss/Cee 7/7 230V 50/60 HZ recalledDatex-OhmedaTemperature AbuseWI
DeviceCLASS IEVair 03 (Jun-air) air compressor recalled by Datex-OhmedaDatex-OhmedaTemperature AbuseWI
DeviceCLASS IIGiraffe OmniBed, with the following recalled by Datex--ohmedaDatex--ohmedaOtherWI
DeviceCLASS IIBeside panel FRU (Field Replacement Units) Kits recalledDatex--ohmedaOtherWI
DeviceCLASS IIGiraffe OmniBed Carestation CS1 recalled by Datex--ohmedaDatex--ohmedaOtherWI
DeviceCLASS IIThe Neonatal Flow Sensor Cable used on devices Carescape recalledDatex-OhmedaDevice MalfunctionNationwide
DeviceCLASS IICarescape R860 ventilators recalled by Datex-OhmedaDatex-OhmedaDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.