Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Nexlizet (bempedoic acid and ezetimibe) Recalled by Esperion Due to Failed dissolution specifications: below specification results at stability...
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 Esperion directly.
Affected Products
Nexlizet (bempedoic acid and ezetimibe), 180ng/18mg, 30 tablets, Rx only, Manufactured for: Esperion Therapeutics, Inc, Ann Arbor, MI 48108, NDC 72426-818-03
Quantity: 45,240 bottles
Why Was This Recalled?
Failed dissolution specifications: below specification results at stability 12-month
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Esperion
Esperion has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report