Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Keppra (levetiracetam) 1000 mg tablets Recalled by Ucb, Inc Due to Failed Dissolution Specifications.
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 Ucb, Inc directly.
Affected Products
Keppra (levetiracetam) 1000 mg tablets, 60 tablets per bottle, Rx only, Manufactured for UCB, Inc. Smyrna, GA 30080, NDC 50474-597-66.
Quantity: 2088 bottles
Why Was This Recalled?
Failed Dissolution Specifications.
Where Was This Sold?
This product was distributed to 1 state: TN
About Ucb, Inc
Ucb, Inc 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