FDA Device recall Z-2518-2018
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
- FDA Device
- Class II
- terminated
- Published 2018-08-01
On 2018-08-01 the FDA classified a Class II recall of Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R by Olympus, citing potential breakage of the endoscope s insertion tube bending section during surgical procedures.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2518-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-01-17 |
| Published | 2018-08-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Olympus |
| Distribution | US |
Product
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Reason
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
Identifiers
| code_info | All Serial Numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2518-2018%22
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