Medical device recalls Moderate risk

Olympus Corporation of the Americas recalls Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip

Recall date
October 22, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1381-2026
FDA classification
Class II
Brand / firm
Olympus Corporation of the Americas
Sold / distributed
Worldwide distribution - US Nationwide and the countries of Brazil, Canada, Germany, Mexico, and Japan.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip

Get recall alerts

Free email alert whenever Olympus Corporation of the Americas has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Olympus Corporation of the Americas