Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R Recalled by Olympus Corporation of the Americas Due to Incorrect adhesive used to secure the diopter ring...
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
Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R
Quantity: 4 units
Why Was This Recalled?
Incorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of vision and unintentional contact with the patients body and in rare cases perforation in the urinary tract/renal pelvis.
Where Was This Sold?
This product was distributed to 8 states: CA, FL, MD, MA, MI, NJ, OH, WI
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