FDA recall Z-1452-2026
Olympus Corporation of the Americas · Class II · device
Product
Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.
Reason for recall
Complaints of the ceramic tip of the resection sheath breaking have been received.
Distribution
US Nationwide Distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2025-11-11
- Report date
- 2026-03-04
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Center Valley, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1452-2026