Bionpharma Inc. recalls Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg
- Recalling company
- Bionpharma Inc.
- 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
- Presence of Foreign Tablets/Capsules
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- Aug 7, 2026
- Reported
- Sep 9, 2026
- Distribution
- US Nationwide.
- Status
- Ongoing
- Quantity
- 14,232 bottles (1,423,200 tablets)
- Lot / codes
- Lot # DMA25006, Exp Date: 11/30/2028.
- Company location
- Princeton, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0822-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0822-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.