Official recall notice
FDA DeviceClass IINotable
FDA Recall: Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applicat
- Recall date
- 2026-03-04
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received.
Recommended action
What to do
9 units
Product description
Complaints of the ceramic tip of the resection sheath breaking have been received.