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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.

Presence of Foreign Tablets/Capsules

Class II Medicine & devices FDA July 29, 2026 Reached Texas
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
Bionpharma Inc. — Princeton, NJ
Severity
Class II — moderate
Reported
July 29, 2026
Quantity
N/A
Recall number
D-0742-2026
Status
Ongoing
Source
FDA

Where it went

US Nationwide.

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