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Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector recall

Olympus Corporation of the Americas recalled Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector on September 30, 2026 because of potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. It was sold nationwide.

Why it was recalled

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

What's recalled

Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA.

Quantity: 404 units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Olympus Corporation of the Americas, Center Valley, PA
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
Worldwide distribution - US Nationwide and the countries of Canada, Latin America, Singapore, Hong Kong, and EU.
Status
Ongoing
Recall number
Z-3244-2026
Source
U.S. Food and Drug Administration

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