Class II

Medical Device Recall: Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.

Olympus Corporation of the Americas · November 11, 2025

Reason for Recall

Complaints of the ceramic tip of the resection sheath breaking have been received.

Distribution

US Nationwide Distribution.

States Affected

NATIONWIDE

Quantity Affected

437 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1450-2026

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 Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications. | SafeCheck