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Olympus Corporation of the Americas recalls Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Recalled March 4, 2026 · FDA recall Z-1437-2026 · Olympus Corporation of the Americas
Hazard
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device. · FDA Class II
Units
633 units
Sold at
Distribution US nationwide.
Description
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
Product
Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →