Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5 Recalled by Olympus Corporation of the Americas Due to Incorrect adhesive used to secure the diopter ring...

Date: April 20, 2022
Company: Olympus Corporation of the Americas
Status: Ongoing
Source: FDA (Device)

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 CYSTONEPHROFIBERSCOPE Model: CYF-5

Quantity: 7 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

Affected (8 states)Not affected

About Olympus Corporation of the Americas

Olympus Corporation of the Americas has 378 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report