Fresh Recalls

Olympus Thunderbeat II Shears w/Ultrasonic Mode: recall status

⚠ Recalls found. Olympus Thunderbeat II Shears w/Ultrasonic Mode is named in 4 official recalls in our current data:

Brand
Olympus of the Americas

Recalls naming this model

FDA Class II · Medical device · April 29, 2026

Olympus Thunderbeat II Shears w/Ultrasonic Mode recall — Olympus Corporation of the Americas

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

Company / brand: Olympus of the Americas

Affected product: Olympus Thunderbeat II Shears w/Ultrasonic Mode

Official ID Z-1851-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Olympus Thunderbeat II Shears w/Ultrasonic Mode recall — Olympus Corporation of the Americas

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

Company / brand: Olympus of the Americas

Affected product: Olympus Thunderbeat II Shears w/Ultrasonic Mode

Official ID Z-1852-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Olympus Thunderbeat II Shears w/Ultrasonic Mode recall — Olympus Corporation of the Americas

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

Company / brand: Olympus of the Americas

Affected product: Olympus Thunderbeat II Shears w/Ultrasonic Mode

Official ID Z-1853-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Olympus Thunderbeat II Shears w/Ultrasonic Mode recall — Olympus Corporation of the Americas

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

Company / brand: Olympus of the Americas

Affected product: Olympus Thunderbeat II Shears w/Ultrasonic Mode

Official ID Z-1854-2026 · Official record ↗

See all Olympus of the Americas recalls →

Verify with the official sources:

Found something wrong or missing? Report a data error.

Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.