FDAClass IIRecall started August 19, 2026

Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector Recall

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

Why was Olympus BiCOAG Hemostasis Probe 7Fr Connector recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Code: Model: CD-B620LA. UDI-DI: 00821925039483. Lot Numbers: All unexpired lots.

Product
Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-B620LA.
Recalling firm
Olympus Corporation of the Americas
Quantity
2,142 units
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Latin America, Singapore, Hong Kong, and EU.
Recall started
August 19, 2026
Report date
September 30, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls