Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
High Frequency Resection Electrodes Recalled by Olympus Corporation of the Americas Due to Loop wires breaking at the distal end of...
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
High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used for endoscopic diagnosis and treatment in urological and gynecological applications.
Quantity: 1264 units
Why Was This Recalled?
Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.
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