Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit
- Recalling company
- Olympus Corporation of the Americas
- Product
- Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
- Reason
- Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 16, 2026
- Reported
- Jul 29, 2026
- Distribution
- Worldwide distribution - US Nationwide and the countries of Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, El Salvador, Germany, Honduras, Hong Kong, India, Ireland, Japan, Korea, Malaysia, Mexico, Myanmar, New Zealand, Paraguay, Peru, Russia, Singapore, Sri Lanka, Taiwan, Thailand, United Kingdom, Uruguay, Vietnam.
- Status
- Ongoing
- Quantity
- 3,087 units
- Lot / codes
- Model Number: UHI-4. UDI: 04953170324147, 04953170467219. All Serial Numbers.
- Company location
- Center Valley, PA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2776-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2776-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.