Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fenoglide (fenofibrate) tablets Recalled by Valeant Pharmaceuticals North America LLC Due to Failed Dissolution Specifications: Failed 24 month dissolution testing.
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 Valeant Pharmaceuticals North America LLC directly.
Affected Products
Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle, Rx Only. Distributed by: Santarus, Inc. San Diego, CA 92130. NDC: 68012-495-90.
Quantity: 3341 Bottles
Why Was This Recalled?
Failed Dissolution Specifications: Failed 24 month dissolution testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Valeant Pharmaceuticals North America LLC
Valeant Pharmaceuticals North America LLC has 25 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report