⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Bionpharma Inc.: Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540,

DrugsSource: FDA (drug) · Date: 2026-07-29

Read the official notice at FDA (drug) →

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The text below is copied from the official FDA (drug) record. If anything differs, the official notice is correct.

Company / brand
Bionpharma Inc.
Product
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.
Reason / hazard
Presence of Foreign Tablets/Capsules
Classification
Class II
Status
Ongoing
Distribution / sold at
US Nationwide.
Recall initiated
2026-06-26
Code info
Lot# 704C003, Exp. 12/31/2028
Product quantity
N/A
Voluntary mandated
Voluntary: Firm initiated
City
Princeton
State
NJ
Country
United States
Event id
99316
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