Class II
Medical Device Recall: Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.
Olympus Corporation of the Americas · November 11, 2025
Reason for Recall
Complaints of the ceramic tip of the resection sheath breaking have been received.
Distribution
US Nationwide Distribution.
States Affected
NATIONWIDE
Quantity Affected
9 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1447-2026
Status: ongoing
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