Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10… — Class III drug recall D-0822-2026
Ongoing recall by Bionpharma Inc., reported 2026-09-09, distributed nationwide. Presence of Foreign Tablets/Capsules
| Recall number | D-0822-2026 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bionpharma Inc., Princeton, NJ, United States |
| Recall initiated | 2026-08-07 |
| Classified | 2026-08-28 |
| Reported by FDA | 2026-09-09 |
| Distributed | Nationwide (US) |
| NDC | 69452-0206, 69452-0206-20 |
| Lot numbers | DMA25006 |
| Expiration dates | 2028-11-30 |
Product
Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg, 100-count bottle, Rx Only, MADE IN INDIA, Distributed by: Bionpharma Inc., Princeton, NJ 08540 NDC 69452-206-20.
Reason for recall
Presence of Foreign Tablets/Capsules
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0822-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.