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Divalproex Sodium Delayed-Release Tablets recall

Bionpharma Inc. recalled Divalproex Sodium Delayed-Release Tablets on July 29, 2026 because of presence of Foreign Tablets/Capsules. It was sold nationwide.

Why it was recalled

Presence of Foreign Tablets/Capsules

What's recalled

Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540, Made in India, NDC 69452-435-30.

Quantity: N/A

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
Bionpharma 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-0742-2026
Source
U.S. Food and Drug Administration

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