Olympus Corporation Of The Americas: Accessories, Cleaning, For Endoscope
Olympus Corporation is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2117) because the lock levers on the Version 2 tubes may fail prematurely. The tubes have been distributed nationwide in the US and in Canada, China, Hong Kong, Japan, South Korea, and Taiwan. This is a Class II recall, meaning the product could cause a serious health problem but is unlikely to cause death.
- Recalling firm
- Olympus Corporation of the Americas
- Product
- OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.
- Reason
- Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-25
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, China, Hong Kong, Japan, South Korea and Taiwan.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1f61ccfa-8bb4-49e5-b3d9-2d65060825a8