Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed Dissolution Specification: This product recall is due...
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 Actavis Elizabeth LLC directly.
Affected Products
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules, 15 mg, Rx Only, C II, 100 capsules per bottle, MFG. By Actavis Elizabeth LLC. 200 Elmora Ave, Elizabeth, NJ, 07207, USA, NDC 0228-3063-11.
Quantity: 9,264 Bottles
Why Was This Recalled?
Failed Dissolution Specification: This product recall is due to the product lot # 50077231 exceeding dissolution specifications. All other test specifications were met.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Actavis Elizabeth LLC
Actavis Elizabeth LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report