Class II

Medical Device Recall: Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;

Olympus Corporation of the Americas · September 13, 2024

Reason for Recall

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.

Distribution

Distribution US nationwide.

States Affected

NATIONWIDE

Quantity Affected

633 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1437-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Olympus Corporation of the Americas Medical Device Recall: Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A; | SafeCheck