Olympus High Flow Insufflation Unit — Class II medical device recall Z-2776-2026
Ongoing recall by Olympus Corporation of the Americas, reported 2026-07-29, distributed nationwide. Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (ins
| Recall number | Z-2776-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2026-06-16 |
| Classified | 2026-07-22 |
| Reported by FDA | 2026-07-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BO, BR, CA, CL, CN, CO, CR, DE, EC, GB, HK, HN, IE, IN, JP, KR, LK, MX, MY, NZ, PE, PY, RU, SG, SV, TH, TW, UY, VN |
| Quantity | 3,087 units |
| UPC / GTIN / UDI-DI | 04953170324147, 04953170467219 |
| Model numbers | UHI-4 |
Product
Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
Reason for recall
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2776-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.