FDAFDA recall Z-3246-2026 · Sep 30, 2026
Olympus Corporation of the Americas: Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector recall
Recall found
Product
Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-B620LA.
Reason for recall
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot Code: Model: CD-B620LA. UDI-DI: 00821925039483. Lot Numbers: All unexpired lots.
- Quantity
- 2,142 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, Latin America, Singapore, Hong Kong, and EU.
- Recalling firm
- Olympus Corporation of the Americas, Center Valley, PA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-08-19
Source: openFDA enforcement record Z-3246-2026 · search recall number Z-3246-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.