Olympus Corporation of the Americas Olympus Uretero-reno videoscope, Model No. URF-V2 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Olympus Uretero-reno videoscope, Model No. URF-V2
Brand
Olympus Corporation of the Americas
Lot Codes / Batch Numbers
1 unit, serial number 2825505F UDI 04953170343582
Products Sold
1 unit, serial number 2825505F UDI 04953170343582
Olympus Corporation of the Americas is recalling Olympus Uretero-reno videoscope, Model No. URF-V2 due to The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.
Recommended Action
Per FDA guidance
On March 25, 2022, the firm contacted the affected consignee to inform them that certain manufacturing changes by a supplier led to the possibility that a part within the bending section may crack. Olympus repaired the affected URF-V2 unit free of charge.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026