Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled by Olympus Corporation of the Americas Due to Complaints of the ceramic tip of the resection...
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 Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.
Quantity: 0 units
Why Was This Recalled?
Complaints of the ceramic tip of the resection sheath breaking have been received.
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