Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode
- Recalling company
- Olympus Corporation of the Americas
- Product
- Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.
- Reason
- Potential for detachment of a distal tip component of the device during use.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 23, 2026
- Reported
- Apr 29, 2026
- Distribution
- International distribution in the countries of Australia, Japan, Hong Kong, and Europe.
- Status
- Ongoing
- Quantity
- 830 units
- Lot / codes
- Model Number: TB2-0520FC. UDI-DI Number: 04953170439995. All Lot Numbers.
- Company location
- Center Valley, PA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1851-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1851-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.