Olympus Corporation of the Americas recalls Olympus Inner Sheath
- Recalling company
- Olympus Corporation of the Americas
- Product
- Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.
- Reason
- Complaints of the ceramic tip of the resection sheath breaking have been received.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Nov 11, 2025
- Reported
- Mar 4, 2026
- Distribution
- US Nationwide Distribution.
- Status
- Ongoing
- Quantity
- 437 units
- Lot / codes
- Model No. WA22017A; UDI: 04042761051514; All Lots.
- Company location
- Center Valley, PA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1450-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1450-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.