RecallHawk
Class II Recall

Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-count bottles (NDC 51407-

Golden State Medical Supply Inc.

Summary

The FDA issued a Class II for Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-2 by Golden State Medical Supply Inc.. Reason: CGMP deviations: tablets with black specks..

Details

Source

Drug Recall

External ID

D-0771-2026

Action Date

2026-08-26

Status

Ongoing

Category

drug

Product Description

Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-count bottles (NDC 51407-215-01), Rx Only, Manufactured by: Taro Pharmaceutical Industries Ltd., Marketed by: GSMS, Incorporated, Camarillo, CA 93012 USA

Lot/Code Info: Lot #: a) GS067429, GS068091, Exp 5/31/2028; b) GS067430, GS068090, Exp 5/31/2028

Quantity Affected: 1200 bottles

Reason for Recall

CGMP deviations: tablets with black specks.

Distribution

USA Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-07

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 42 drug recalls issued in the same week, part of 66 drug-related FDA actions this month.

Golden State Medical Supply Inc. has 25 FDA actions in our database, including 25 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Golden State Medical Supply Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Golden State Medical Supply Inc. have FDA actions?

Golden State Medical Supply Inc. has 25 FDA actions in our database, including 25 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0771-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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