Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R — Class II medical device recall Z-2518-2018
Terminated recall by Olympus Corporation of the Americas, reported 2018-08-01, distributed nationwide. Potential breakage of the endoscope s insertion tube bending section during surgical procedures
| Recall number | Z-2518-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2018-01-17 |
| Classified | 2018-07-20 |
| Reported by FDA | 2018-08-01 |
| Terminated | 2019-12-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 2,548 |
| Reason classes | device malfunction |
Product
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Reason for recall
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
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-2518-2018. 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.