CLASS II Drug recall · Reported 2 Feb 2022 · FDA Enforcement Report

Metoprolol Succinate Extended-Release Tablets, USP, 25 mg recalled

Ascend Laboratories is recalling Metoprolol Succinate Extended-Release Tablets, USP, 25 mg, distributed nationwide in the US. The recall was initiated on 12 Jan 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 21143093, Exp. March 2023
NDC67877-590, 67877-591, 67877-592, 67877-593
Quantity recalled9216 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0393-2022
FDA event ID
89411
Recalling firm
Ascend Laboratories, Parsippany, NJ
Manufacturer
Ascend Laboratories, LLC
Classification
Class II
Status
Terminated
Recall initiated
12 Jan 2022
FDA classified
21 Jan 2022
Reported
2 Feb 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

12 Jan 2022Recall initiated by company
21 Jan 2022Classified by FDA+9 days
2 Feb 2022Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Failed Dissolution Specifications.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Metoprolol Succinate Extended-Release Tablets, USP, 25 mg, Rx Only, 100 Tablets per bottle, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ, 07054, NDC 67877-590-01.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Failed Dissolution Specifications.

Which lots are affected?

Lot #: 21143093, Exp. March 2023

Where was it sold?

Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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