- Recalling firm
- Olympus Corporation of the Americas
- Reason for recall
- Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Affected products (lot / model / serial)
- Model Number: MAJ-2138. UDI Number: 04953170404184. Lot Numbers: 09A, 0XA, 0YA, 0ZA, 11A, 12A, 24A, 25A, 26A, 27A, 28A, 29A, 2XA, 2YA, 3XA, 3YA, 3ZA, 41A, 42A, 43A, 44A, 45A, 46A, 47A, 48A, 49A, 4XA, 4YA, 4ZA, 51A.
- Units affected
- 808 units
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Canada, China, Hong Kong, Japan, South Korea and Taiwan.
- 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-1908-2026
- Recall initiated
- March 25, 2026
- FDA classification date
- April 22, 2026
- FDA report date
- April 29, 2026
- FDA event ID
- 98544
- Last updated on HTM Vibe
- July 24, 2026