Class II

Medical Device Recall: Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-B620LA.

Olympus Corporation of the Americas · August 19, 2026

Reason for Recall

Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Latin America, Singapore, Hong Kong, and EU.

States Affected

NATIONWIDE

Quantity Affected

2,142 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3246-2026

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 BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-B620LA. | SafeCheck