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.