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Uhi-3 high flow insufflation system - insufflator
Official notice
6 Feb 2026
Last checked
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 VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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Affected products
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Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
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Company & contacts
Company & contacts
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Brand: Olympus Medical.
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Source & status
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Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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