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Olympus Corporation of the Americas recalls Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.
Recalled March 4, 2026 · FDA recall Z-1453-2026 · Olympus Corporation of the Americas
Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received. · FDA Class II
Units
1 unit
Sold at
US Nationwide Distribution.
Description
Complaints of the ceramic tip of the resection sheath breaking have been received.
Product
Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →