Olympus MAJ-210 Biopsy Valve Recall
Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instru
Updated January 29, 2026
Olympus single-use biopsy valves (Model MAJ-210) may shed rubber fragments during use. Healthcare providers should stop using affected units and contact Olympus to arrange a replacement.
Is the Olympus Corporation of the Americas recalled? Yes. This product was recalled by FDA on January 29, 2026. Details below.
What is recalled
Olympus Single use Biopsy Valve, Model/Catalog Number MAJ-210, 20 units per box. This valve attaches to the instrument channel port of compatible endoscopes.
Am I affected
You are affected if you are a healthcare facility or endoscopy provider that has received or is using Olympus MAJ-210 biopsy valves (20-unit boxes).
What to do right now
Stop using MAJ-210 biopsy valves immediately. Contact Olympus Corporation of the Americas to arrange a replacement for affected units.
The hazard
Potential for rubber fragment detachment during use.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1488-2026
- Classification
- Class II
- Recalled
- January 29, 2026
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