Class II

Medical Device Recall: Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A.

Olympus Corporation of the Americas · May 5, 2026

Reason for Recall

Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Japan, EU, and Latin America.

States Affected

NATIONWIDE

Quantity Affected

3,663 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2721-2026

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: Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A. | SafeCheck