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The official notice did not include a photo. Check the product details and identifiers below.
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Uhi-3 high flow insufflation system - insufflator
Official notice
6 Feb 2026
An official Health Canada notice concerns Uhi-3 high flow insufflation system - insufflator. 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. Published 2026-02-06.
What to do now
Contact the manufacturer if you require additional information.
Recall number
81573
Official notice
2026-02-06
The hazard
The hazard
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.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Olympus Medical.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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