Olympus Corporation of the Americas recalled the Resection Sheath Model A2666T on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard for patients. Healthcare providers and patients should stop using the device immediately.
Complaints of the ceramic tip of the resection sheath breaking have been received.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Olympus Corporation of the Americas or your healthcare provider for instructions. Notification method: Letter
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The recalled product is the Olympus Resection Sheath, Model No. A2666T. It is used for endoscopic diagnosis and treatment in urological applications. This recall affects all lots of the device.
The ceramic tip of the resection sheath may break during use, which can lead to serious complications during medical procedures. This recall has been classified as Class II by the FDA, indicating a moderate risk.
There have been complaints reported regarding the ceramic tip breaking. No specific injury or incident counts have been disclosed.
Stop using the resection sheath immediately. Follow the recall instructions sent via letter and contact Olympus Corporation of the Americas or your healthcare provider for further guidance.
For more details, contact Olympus Corporation of the Americas. Visit their official website or call the provided contact number for assistance.
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