FDAClass IIMarch 4, 2026

Olympus Resection Sheath recall

Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications.

Why was Olympus Resection 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. A22043T; UDI: 04042761021012; All Lots.

Product
Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications.
Recalling firm
Olympus Corporation of the Americas
Quantity
207 units
Distribution
US Nationwide Distribution.
Recall date
March 4, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls