Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Prevacid 24HR (Lansoprazole) delayed-release capsules Recalled by GLAXOSMITHKLINE NEBRASKA Due to CGMP deviations
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 GLAXOSMITHKLINE NEBRASKA directly.
Affected Products
Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.
Quantity: 5,548,673 bottles
Why Was This Recalled?
CGMP deviations
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GLAXOSMITHKLINE NEBRASKA
GLAXOSMITHKLINE NEBRASKA has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report