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Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.
Recalled March 4, 2026 · FDA recall Z-1449-2026 · Olympus Corporation of the Americas
Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received. · FDA Class II
Units
91 units
Sold at
US Nationwide Distribution.
Description
Complaints of the ceramic tip of the resection sheath breaking have been received.
Product
Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →