Olympus Uretero-reno videoscope — Class II medical device recall Z-1116-2022
Ongoing recall by Olympus Corporation of the Americas, reported 2022-05-25, distributed nationwide. The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bend
| Recall number | Z-1116-2022 |
|---|---|
| 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 | 2022-03-25 |
| Classified | 2022-05-19 |
| Reported by FDA | 2022-05-25 |
| Distributed | Nationwide (US) |
| Quantity | 1 |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 04953170343582 |
| Serial numbers | 2825505F |
| Model numbers | URF-V2 |
Product
Olympus Uretero-reno videoscope, Model No. URF-V2
Reason for recall
The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.
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-1116-2022. 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.