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Medium risk Medical DevicesClass II

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

Olympus Corporation of the Americas
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1488-2026
Classification
Class II
Recalled
January 29, 2026
Read the official notice

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