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Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Dis… Recalled: Presence of Foreign Tablets/Capsules

Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500… was recalled on June 26, 2026 in cooperation with the U.S. Food and Drug Administration because presence of Foreign Tablets/Capsules.

Is my unit affected?

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.

Model, lot & date codes to check

Lot# 704C003, Exp. 12/31/2028

Units affected: N/A

Where it was sold: US Nationwide.

Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.

What's the hazard?

Presence of Foreign Tablets/Capsules

Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.

Your remedy & how to claim it

Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.

Contact: Recalling firm: Bionpharma Inc.

Not sure what you're entitled to? Read our guide: what to do if your product is recalled.

Official recall notice

Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.

View official notice →

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