FDA Device recall Z-1116-2022
Olympus Uretero-reno videoscope, Model No. URF-V2
- FDA Device
- Class II
- ongoing
- Published 2022-05-25
On 2022-05-25 the FDA classified a Class II recall of Olympus Uretero-reno videoscope, Model No. URF-V2 by Olympus, citing the bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1116-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-03-25 |
| Published | 2022-05-25 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Olympus |
| Distribution | US |
Product
Olympus Uretero-reno videoscope, Model No. URF-V2
Reason
The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.
Identifiers
| code_info | 1 unit, serial number 2825505F UDI 04953170343582 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1116-2022%22
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