Ascend Laboratories recalls Metoprolol Succinate Extended-Release Tablets, 25 mg, over failed dissolution specifications
The tablets failed dissolution specifications, and the notice covers 17,304 100-count bottles sold across the U.S.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- 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.
- Company
- Ascend Laboratories, LLC
- Hazard
- Failed Dissolution Specifications
- Units
- 17,304 100-count bottles
- Where sold
- U.S. Nationwide
- FDA classification
- Class II · Ongoing
- Classified by FDA
- May 20, 2026
- Recall started
- April 27, 2026
- FDA enforcement report
- May 20, 2026
- Identifiers
- Codes: Lot # 25140859; Exp. Date: Jan 2027
- FDA recall number: D-0547-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- 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 for recall
- Failed Dissolution Specifications
- Classification
- Class II (Ongoing)
- Distribution
- U.S. Nationwide
- Quantity
- 17,304 100-count bottles
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