FDA · Drugs ·
Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg recall
Bionpharma Inc. recalled Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg on September 9, 2026 because of presence of Foreign Tablets/Capsules. It was sold nationwide.
Why it was recalled
Presence of Foreign Tablets/Capsules
What's recalled
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.
Quantity: 14,232 bottles (1,423,200 tablets)
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Bionpharma Inc., Princeton, NJ
- Date
- Severity
- Class III
the product is unlikely to cause health problems but breaks a rule. - Where sold
- Nationwide
US Nationwide. - Status
- Ongoing
- Recall number
- D-0822-2026
- Source
- U.S. Food and Drug Administration
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