Unlikely to cause harm — often a labeling or packaging issue.
Presence of Foreign Tablets/Capsules
| Brand name | DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE |
| Generic name | DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE |
| Active ingredient(s) | DOXYLAMINE SUCCINATE, PYRIDOXINE HYDROCHLORIDE |
| Distributed by / for | Bionpharma Inc., Princeton, NJ 08540 |
| NDC | 69452-206-20 |
| Full product label | 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. |
| Recalling firm | Bionpharma Inc. |
| Distribution | US Nationwide. |
| Quantity | 14,232 bottles (1,423,200 tablets) |
| Recall initiated | 2026-08-07 |
| Report date | 2026-09-09 |
| Recall completed | — |
| Recall number | D-0822-2026 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Princeton NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗