Olympus High Flow Insufflation Unit recall: Software Issue
Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to…
Why was Olympus High Flow Insufflation Unit recalled?
Issue with software algorithm which may lead to overpressure events.
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; UDI-DI: N/A; All Serial Numbers
- Product
- Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to…
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 18 units
- Distribution
- Nationwide distribution
- Recall date
- February 25, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)