Niacin: 6 recalls on record
Recalled by 1 agency: FDA (6).
First recall on record: January 31, 2024. Most recent: June 17, 2026.
Risk classification: Class II: 6
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| June 17, 2026 | FDA | GSMS Incorporated, NIACIN EXTENDED-RELEASE TABLETS, USP, 1,000 MG, 90 tablets, Rx only, M…D-0587-2026 | D-0587-2026 |
| June 10, 2026 | FDA | Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by…D-0584-2026 | D-0584-2026 |
| November 26, 2025 | FDA | NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactu…D-0158-2026 | D-0158-2026 |
| October 29, 2025 | FDA | Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distribut…D-0096-2026 | D-0096-2026 |
| January 31, 2024 | FDA | Niacin Extended-Release Tablets, USP 500mg, Rx Only, 90 Tablets per bottle, Distributed b…D-0270-2024 | D-0270-2024 |
| January 31, 2024 | FDA | Niacin Extended-Release Tablets, USP 1000mg, Rx Only, 90 Tablets per bottle, Distributed …D-0269-2024 | D-0269-2024 |
Questions about this brand
- How many recalls does Niacin have?
- Recalert has 6 U.S. recalls on record for Niacin, published between January 31, 2024 and June 17, 2026.
- What was the most recent Niacin recall?
- FDA recall D-0587-2026, published June 17, 2026: GSMS Incorporated, NIACIN EXTENDED-RELEASE TABLETS, USP, 1,000 MG, 90 tablets, Rx only, Manufactured by Kremers Urban Pharmaceuticals Inc., a subsidiary of Lannett, Inc., Seymour, IN 47274, Packaged …
- Which agencies have recalled Niacin products?
- Niacin products appear in recalls from: FDA (6).
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