Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Metoprolol Succinate Extended-Release Tablets Recalled by Amerisource Health Services LLC Due to Failed Dissolution Specifications: This recall is being initiated...
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 Amerisource Health Services LLC directly.
Affected Products
Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, packaged in (a) 100-count bottle, NDC 68001-501-00; (b) 500-count bottle, NDC 68001-501-03. Manufactured by Alkem Laboratories Ltd., India. For BluePoint Laboratories
Quantity: (a) 6670 100-count (b) 2666 500-count bottles
Why Was This Recalled?
Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Amerisource Health Services LLC
Amerisource Health Services LLC has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report