Official recall record
UHI-3 High Flow Insufflation System - Insufflator
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-02-06
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Olympus is initiating a Medical Device Recall on the High Flow Insufflation Unit Models UHI, UHI-2, UHI-3, and UHI-E. Olympus is requesting customers to immediately cease usage of the affected devices and contact customer service to return their affected products. *Note* These products have been discontinued for sale and repair.
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 2026-05-31.
Record last checked against the registry on 2026-05-31.
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