FDA recall D-0742-2026

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 for recall

Presence of Foreign Tablets/Capsules

Distribution

US Nationwide.

Key facts

Status

Ongoing

Initiation date

2026-06-26

Report date

2026-07-29

Voluntary/Mandated

Voluntary: Firm initiated

Location

Princeton, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0742-2026