FDA · Medical devices ·
Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector recall
Olympus Corporation of the Americas recalled Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin 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 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA.
Quantity: 816 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 noticeDetails
- 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-3247-2026
- Source
- U.S. Food and Drug Administration
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