Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by Olympus Corporation of the Americas Due to Potential breakage of the endoscope s insertion tube...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Olympus Corporation of the Americas directly.
Affected Products
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Quantity: 2548
Why Was This Recalled?
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Olympus Corporation of the Americas
Olympus Corporation of the Americas has 378 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report