Olympus Corporation Of The Americas: Accessories, Cleaning, For Endoscope

Recall Summary Olympus Corporation of the Americas is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2119) distributed worldwide, including across all US states and several other countries. The lock levers on Version 2 of these tubes may fail prematurely. This is classified as a Class II recall, indicating a potential serious health issue.

Recalling firm
Olympus Corporation of the Americas
Product
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.
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/be5c0e07-f354-4ce7-821f-7a67774b1c5e