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