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Olympus Corporation of the Americas recalls Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to
Recalled March 11, 2026 · FDA recall Z-1489-2026 · Olympus Corporation of the Americas
Hazard
Potential for rubber fragment detachment during use. · FDA Class II
Units
1,276 boxes (20 units 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-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent leakage of body fluids.
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →