FDA Drug recall D-0742-2026
Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540,…
- FDA Drug
- Class II
- ongoing
- Published 2026-07-29
On 2026-07-29 the FDA classified a Class II recall of Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540,… by Bionpharma, citing presence of Foreign Tablets/Capsules.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0742-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-26 |
| Published | 2026-07-29 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Bionpharma |
| Distribution | US |
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
Identifiers
| ndc | 69452-433-13 |
|---|---|
| ndc | 69452-433-20 |
| ndc | 69452-433-30 |
| ndc | 69452-434-13 |
| ndc | 69452-434-20 |
| ndc | 69452-434-30 |
| ndc | 69452-435-13 |
| ndc | 69452-435-20 |
| ndc | 69452-435-30 |
| code_info | Lot# 704C003, Exp. 12/31/2028 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0742-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.