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FDA DeviceClass IINotable

FDA Recall: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 h

Date: 2026-03-11
Brand: Olympus Corporation of the Americas
Category: Medical Device
FDA Class: Class II

Description

Potential for rubber fragment detachment during use.

Hazard

Potential for rubber fragment detachment during use.

Remedy

1,276 boxes (20 units per box)

View original recall →
FDA Recall: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 h | RecallWatch