- Recalling firm
- Olympus Corporation of the Americas
- Reason for recall
- Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
- Affected products (lot / model / serial)
- Model Number: CD-B610LA. UDI-DI: 00821925039469. Lot Numbers: All unexpired lots.
- Units affected
- 404 units
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Canada, Latin America, Singapore, Hong Kong, and EU.
- Firm location
- Center Valley, PA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3244-2026
- Recall initiated
- August 19, 2026
- FDA classification date
- September 18, 2026
- FDA report date
- September 30, 2026
- FDA event ID
- 99609
- Last updated on HTM Vibe
- October 6, 2026
