Uretero-reno fiberscope URF-P6RP6 — Class II medical device recall Z-2520-2018
Terminated recall by Olympus Corporation of the Americas, reported 2018-08-01, distributed nationwide. Breakage of the endoscope's insertion tube bending section during surgical procedures.
| Recall number | Z-2520-2018 |
|---|---|
| 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, MX |
| Quantity | 2,399 |
| Reason classes | device malfunction |
Product
Uretero-reno fiberscope URF-P6RP6
Reason for recall
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-2520-2018. 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.