Class II

Medical Device 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 instrument channel port of compatible endoscopes to prevent ref

Olympus Corporation of the Americas · January 29, 2026

Reason for Recall

Potential for rubber fragment detachment during use.

Product Description

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.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

95,882 boxes (20 per box)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1488-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.