Olympus High Flow Insufflation Unit - UHI-4 recall
Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
Why was Olympus High Flow Insufflation Unit - UHI-4 recalled?
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model Number: UHI-4. UDI: 04953170324147, 04953170467219. All Serial Numbers.
- Product
- Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 3,087 units
- 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.
- Recall date
- July 29, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)