{"url_path":"/fda/device/recalls/Z-2776-2026","section_key":"summary","section_title":"DEVICE Recall: Olympus Corporation of the Americas — Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-16","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2776-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Olympus Corporation of the Americas"},"word_count":117,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2776-2026\n\n**Recalling firm:** Olympus Corporation of the Americas\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-06-16\n**Report date:** 2026-07-29\n\n## Product\nOlympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4\n\n## Reason\nPotential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.\n\n## Affected lots\nModel Number: UHI-4. UDI: 04953170324147, 04953170467219. All Serial Numbers.\n\n## Distribution\nWorldwide 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."}