Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units Recalled by Olympus Corporation of the Americas Due to Potential for rubber fragment detachment during use.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Olympus Corporation of the Americas directly.
Affected Products
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.
Quantity: 1,276 boxes (20 units per box)
Why Was This Recalled?
Potential for rubber fragment detachment during use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Olympus Corporation of the Americas
Olympus Corporation of the Americas has 378 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report