CLASS II Drug recall · Reported 19 Jan 2022 · FDA Enforcement Report

Carbamazepine Tablets, USP 200 mg recalled by Torrent Pharma

Torrent Pharma is recalling Carbamazepine Tablets, USP 200 mg, distributed nationwide in the US. The recall was initiated on 2 Dec 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch: 4J11G002 Exp. 08/2024
NDC13668-268, 13668-271
Quantity recalled15,336 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-0365-2022
FDA event ID
89146
Recalling firm
Torrent Pharma, Basking Ridge, NJ
Manufacturer
Torrent Pharmaceuticals Limited
Classification
Class II
Status
Terminated
Recall initiated
2 Dec 2021
FDA classified
11 Jan 2022
Reported
19 Jan 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

2 Dec 2021Recall initiated by company
11 Jan 2022Classified by FDA+40 days
19 Jan 2022Published in enforcement report+8 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 Tablets, USP 200 mg 100 Tablets Rx only NDC 13668-268-01 Manufactured by: Torrent Pharmaceuticals Ltd. Bharuch-392130, India Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920.

Where it was distributed

Nationwide USA

Nationwide

Questions about this recall

Why was it recalled?

Failed Dissolution Specifications

Which lots are affected?

Batch: 4J11G002 Exp. 08/2024

Where was it sold?

Nationwide 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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