Olympus Inner Sheath recall
Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.
Why was Olympus Inner Sheath recalled?
Complaints of the ceramic tip of the resection sheath breaking have been received.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model No. A2641; UDI: 04042761004060; All Lots.
- Product
- Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 0 units
- Distribution
- US Nationwide Distribution.
- Recall date
- March 4, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)