Official recall record
GE Healthcare Integrated and Stand-Alone Resuscitation systems
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-06-16
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
GE HealthCare has become aware of a potential issue involving the air-oxygen blender knob shaft on certain (serial number specific) integrated and stand-alone Resuscitation systems. In some cases, the blender knob shaft can loosen, which can affect the delivered oxygen concentration. If this occurs, 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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-06-26.
Record last checked against the registry on 2026-06-26.
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