Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
FDA Recall Z-1353-2026 · Posted 2026-02-18
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Recalling FirmOlympus Corporation of the Americas
Recall StatusOpen, Classified
Product CodeHIF
Date Initiated2026-01-16
Product Quantity744 units
Reason for Recall
Issue with software algorithm which may lead to overpressure events.
Firm Action
Olympus notified consignees on about 01/16/2026 via "URGENT: MEDICAL DEVICE REMOVAL" letter. Consignees were instructed to cease usage of the affected product immediately. They are advised to use available alternatives including an existing UHI-4 if available or switching to an insufflation device from another manufacturer. If no alternative is available on site, contact Olympus to arrange a loaner or purchase a replacement.
Additionally, consignees were instructed to examine inventory and quarantine any identified devices, immediately cease usage of any UHI, UHI-2, and/or UHI-3 in inventory, call Olympus Customer Service at 1-800-848-9024, option 2 to obtain a Return Material Authorization to return your device. Consignees were also requested to acknowledge receipt of this letter through their recall web portal as follows: a. Go to https://olympusamerica.com/recall, b. Enter the recall number "0489 and c. Complete the form as instructed. Please indicate in your response if you no longer have the device(s).
If any consignees have further distributed this UHI product, they were instructed to identify affected customers and forward this notice to them immediately.
If you require additional information, please do not hesitate to contact me by phone at (647) 999-3203 or by email at [email protected].
Root Cause
Software design
Distribution Pattern
Nationwide distribution
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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