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Medium risk Drugs & MedicationsClass II

Olympus Corporation of the Americas 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 Corporation of the Americas is recalling 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. Hazard: Potential for rubber fragment detachment during use.

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. The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent reflux of body fluids.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

Potential for rubber fragment detachment during use.

Brands affected

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

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