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FDA · Drugs ·

Ascend Laboratories recall

Ascend Laboratories, LLC recalled Ascend Laboratories on May 20, 2026 because of failed dissolution specifications. It was sold nationwide.

Why it was recalled

Failed Dissolution Specifications

What's recalled

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.

Quantity: 17,304 100-count bottles

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Ascend Laboratories, LLC, Bedminster, NJ
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
U.S. Nationwide
Status
Ongoing
Recall number
D-0547-2026
Source
U.S. Food and Drug Administration

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