Divalproex Sodium: 6 recalls on record

Recalled by 1 agency: FDA (6).

First recall on record: January 24, 2018. Most recent: July 29, 2026.

Risk classification: Class II: 6

Most recent recalls

DateAgencyProduct
July 29, 2026FDADivalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Dis…D-0742-2026
April 3, 2024FDADivalproex Sodium Extended-release Tablets, USP 250 mg, Rx Only, 100 tablets, Manufacture…D-0426-2024
August 31, 2022FDADivalproex Sodium Extended Release Tablets, USP, 250 mg, packaged in 100-count bottle, Rx…D-1362-2022
August 3, 2022FDADivalproex Sodium Delayed-Release Tablets, USP 500mg, Rx Only, 100 Tablets, Distributed b…D-1291-2022
February 27, 2019FDADivalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only, Mfd.By…D-0507-2019
January 24, 2018FDADivalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufac…D-0228-2018

Questions about this brand

How many recalls does Divalproex Sodium have?
Recalert has 6 U.S. recalls on record for Divalproex Sodium, published between January 24, 2018 and July 29, 2026.
What was the most recent Divalproex Sodium recall?
FDA recall D-0742-2026, published July 29, 2026: 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.
Which agencies have recalled Divalproex Sodium products?
Divalproex Sodium products appear in recalls from: FDA (6).

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