Ascend Laboratories, Llc, Metoprolol Succinate Extended-release Tablets, Usp, 25 Mg*

Metoprolol Succinate Recall Summary Ascend Laboratories is recalling Metoprolol Succinate Extended-Release Tablets 25 mg nationwide because the tablets failed dissolution testing, meaning they may not break down properly in the body to deliver the medication as intended. This recall affects the specific product manufactured by Alkem Laboratories Ltd. in India and distributed by Ascend Laboratories. The recall was distributed across all U.S. states and territories.

Recalling firm
Ascend Laboratories, LLC
Product
Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-590-01.
Reason
Failed Dissolution Failure
Category
drug recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-04-27
Status
Ongoing
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
U.S. Nationwide

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/68d9c3ee-69e5-44f5-9bf3-f967c5998d4d