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Olympus Corporation of the Americas recalls Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be
Recalled March 11, 2026 · FDA recall Z-1488-2026 · Olympus Corporation of the Americas
Hazard
Potential for rubber fragment detachment during use. · FDA Class II
Units
95,882 boxes (20 per box)
Sold at
US Nationwide distribution.
Description
Potential for rubber fragment detachment during use.
Product
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.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →