Class II

Medical Device Recall: Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated 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

0 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1376-2026

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 Thunderbeat 5 mm, 20 cm, Front-Actuated Grip | SafeCheck