Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ethosuximide Capsules Recalled by Akorn, Inc. Due to Failed Impurities/Degradation Specifications: Out of specification (OOS) results...
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 Akorn, Inc. directly.
Affected Products
Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA 30062. Mfg By: Swiss Caps AG, Kirchberg, Switzerland. NDC: 61748-025-01
Quantity: 23,788 100-count bottles
Why Was This Recalled?
Failed Impurities/Degradation Specifications: Out of specification (OOS) results for unspecified impurity.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akorn, Inc.
Akorn, Inc. has 176 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report