Medical device recalls Moderate risk

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.

Recall date
March 25, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1907-2026
FDA classification
Class II
Brand / firm
Olympus Corporation of the Americas
Sold / distributed
Worldwide distribution - US Nationwide and the countries of Canada, China, Hong Kong, Japan, South Korea and Taiwan.

Why it was recalled

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.

Get recall alerts

Free email alert whenever Olympus Corporation of the Americas has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Olympus Corporation of the Americas