Class II

Medical Device Recall: Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip

Olympus Corporation of the Americas · October 22, 2025

Reason for Recall

Firm is initiating a removal due to continued reports of adverse events.

Distribution

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, Germany, Mexico, and Japan.

States Affected

NATIONWIDE

Quantity Affected

3,381 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1378-2026

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.