CLASS II ONGOING Drug recall · Reported 8 Oct 2025 · FDA Enforcement Report

Carbamazepine Extended-Release Tablets recalled

Amerisource Health Services is recalling Carbamazepine Extended-Release Tablets, USP 400 mg per carton ( unit dose cards), distributed nationwide in the US. The recall was initiated on 15 Sep 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 1024078, Exp. Date 08/31/2026
NDC60687-583, 60687-594
Quantity recalled360 cartons

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-0675-2025
FDA event ID
97634
Recalling firm
Amerisource Health Services, Columbus, OH
Manufacturer
American Health Packaging
Classification
Class II
Status
Ongoing
Recall initiated
15 Sep 2025
FDA classified
29 Sep 2025
Reported
8 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

15 Sep 2025Recall initiated by company
29 Sep 2025Classified by FDA+14 days
8 Oct 2025Published in enforcement report+9 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

Carbamazepine Extended-Release Tablets, USP 400 mg, 30 Tablets per carton (3x10 unit dose cards), Rx Only, American Health Packaging, Columbus, OH 43217. Carton NDC 60687-594-21; (Individual Dose NDC: 60687-594-11)

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 #: 1024078, Exp. Date 08/31/2026

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.

More recalls from Amerisource Health Services

All 69

Other Carbamazepine recalls

All 13