Class II

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

Olympus Corporation of the Americas · March 25, 2026

Reason for Recall

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

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, China, Hong Kong, Japan, South Korea and Taiwan.

States Affected

NATIONWIDE

Quantity Affected

741 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1907-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Olympus Corporation of the Americas Medical Device Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119. | SafeCheck