Lannett Company Inc. 2025-10-29 Health serious FDA
Health · FDA · Recall #FDA-D-0096-2026
Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle,… Recall
Issued October 29, 2025 · Lannett Company Inc.
In October 2025, Lannett Company Inc. recalled the Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed Dissolution Specifications
What you should do
- 1 Stop using Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Lannett Company Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Lannett Company Inc.
- Category
- Health
- Recall date
- October 29, 2025
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0096-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Lannett Company Inc. has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.