Medical device recalls Moderate risk

Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.

Recall date
March 23, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1851-2026
FDA classification
Class II
Brand / firm
Olympus Corporation of the Americas
Sold / distributed
International distribution in the countries of Australia, Japan, Hong Kong, and Europe.

Why it was recalled

Potential for detachment of a distal tip component of the device during use.

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 II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.

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