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GE Healthcare Integrated and Stand-Alone Resuscitation systems — recall 82212

Health Canada — Medical Devices · Canada · 2026-06-16 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 82212
Date of alert: 2026-06-16
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: General hospital and personal use
Product type: Medical devices

Reported risk: 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.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/ge-healthcare-integrated-and-s

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GE Healthcare Integrated and Stand-Alone Resuscitation systems — recall 82212

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