medical MODERATE Updated 2026-09-30

Olympus Corporation of the Americas recalls Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model

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Recalled Product

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

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Code: Model: CD-B620LA. UDI-DI: 00821925039483. Lot Numbers: All unexpired lots.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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