Datex-ohmeda, Inc.
3030 Ohmeda Drive, MADISON, WI, US
Registered product codes
8 product codes
Recent MDR events
52,444 on file
- CARESCAPEJul 31, 2026Malfunction2112667-2026-04804
- AESPIREJul 31, 2026Malfunction2112667-2026-04805
- AvanceJul 31, 2026Malfunction2112667-2026-04806
- AvanceJul 31, 2026Malfunction2112667-2026-04807
- ENGSTROMJul 31, 2026Malfunction2112667-2026-04808
- AvanceJul 31, 2026Malfunction2112667-2026-04809
- AisysJul 31, 2026Malfunction2112667-2026-04810
- AisysJul 31, 2026Malfunction2112667-2026-04811
- AisysJul 31, 2026Malfunction2112667-2026-04812
- Carestation 620Jul 31, 2026Malfunction2112667-2026-04813
Recalls
55 on file
- Open, ClassifiedJun 18, 2026
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
View FDA record ↗ - Open, ClassifiedJun 18, 2026
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
View FDA record ↗ - Open, ClassifiedJun 18, 2026
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
View FDA record ↗ - CompletedOct 31, 2024
Prior to current established manufacturing practices, higher levels of airborne formaldehyde exposure from newly manufactured incubators could be seen during clinical use that would rapidly decrease over a week. Affected customers were notified in June 2023 to run incubators for a week to potentially off gas any residual airborne formaldehyde. The general scientific consensus is that sensory irritation of the eyes is the most sensitive endpoint with respect to exposure to airborne formaldehyde and is the adverse effect clinically experienced at the lowest concentration.
View FDA record ↗ - CompletedOct 31, 2024
Prior to current established manufacturing practices, higher levels of airborne formaldehyde exposure from newly manufactured incubators could be seen during clinical use that would rapidly decrease over a week. Affected customers were notified in June 2023 to run incubators for a week to potentially off gas any residual airborne formaldehyde. The general scientific consensus is that sensory irritation of the eyes is the most sensitive endpoint with respect to exposure to airborne formaldehyde and is the adverse effect clinically experienced at the lowest concentration.
View FDA record ↗ - Open, ClassifiedOct 18, 2024
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
View FDA record ↗ - Open, ClassifiedOct 18, 2024
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
View FDA record ↗ - Open, ClassifiedOct 18, 2024
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
View FDA record ↗ - Open, ClassifiedOct 18, 2024
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
View FDA record ↗ - Open, ClassifiedOct 18, 2024
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
View FDA record ↗
Compliance history
Matched by FEI 2112667.
FDA inspections
1 on file
- Voluntary Action Indicated (VAI)Nov 17, 2023
Compliance: Devices · Citations posted
Inspection citations
1 on file
Top cited requirements
Compare to industry ↗- 21 CFR 820.100(a)Nov 17, 2023
Lack of or inadequate procedures
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
1 on file
Top refusal reasons
Compare to industry ↗- Division of Northern Border Imports (DNBI)Oct 10, 2025
73CAD \ VAPORIZER, ANESTHESIA, NON-HEATED