Bionpharma Inc.: Divalproex Sodium Delayed-release Tablets, Usp, 500 Mg, 500 Tablets Bottles
Recall Summary Bionpharma Inc. is recalling bottles of Divalproex Sodium Delayed-Release Tablets, 500 mg (NDC 69452-435-30), distributed nationwide because some bottles contain foreign tablets or capsules mixed in with the medication. This is a prescription medication used to treat seizures and other conditions. The recall affects patients who received this product across all U.S. states and Washington, D.C.
- Recalling firm
- 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
- Presence of Foreign Tablets/Capsules
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-06-26
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/e58a0d7a-ab7a-4719-921b-1785a0384237