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Olympus Corporation of the Americas recalls Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.
Recalled March 4, 2026 · FDA recall Z-1451-2026 · Olympus Corporation of the Americas
Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received. · FDA Class II
Units
1,141 units
Sold at
US Nationwide Distribution.
Description
Complaints of the ceramic tip of the resection sheath breaking have been received.
Product
Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →