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FDA · Drugs ·

Carbamazepine Tablets recall

SUN PHARMACEUTICAL INDUSTRIES INC recalled Carbamazepine Tablets on August 26, 2026 because of cGMP Deviations; black spots found on tablets from burnt excipient during manufacturing. It was sold nationwide.

Why it was recalled

CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing

What's recalled

Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Distributed by: Taro Pharmaceuticals USA, Inc., Hawthorne, NY 10532, NDC 51672-4005-3.

Quantity: 1968 Bottles (1000Tablets/Bottle)

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
SUN PHARMACEUTICAL INDUSTRIES INC, Princeton, NJ
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide.
Status
Ongoing
Recall number
D-0770-2026
Source
U.S. Food and Drug Administration

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