Lannett recalls

9 official recalls and safety alerts involving Lannett since 2022-02, from FDA · Drug. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Lannett or the relevant agency.

  1. 2026-07-08
  2. US
    Drugs & medicalClass II

    Lannett Company Inc. recalls Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release…

    Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.

    FDA · DrugLannett Company Inc.US Nationwide.Official notice →
  3. 2026-06-10
  4. US
    Drugs & medicalClass II

    Lannett Company Inc. recalls Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136,…

    Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.

    FDA · DrugLannett Company Inc.Nationwide within the United StatesOfficial notice →
  5. 2026-05-27
  6. US
    Drugs & medicalClass III

    Lannett Company Inc. recalls Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1231-01.

    Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

    FDA · DrugLannett Company Inc.USA NationwideOfficial notice →
  7. 2025-10-29
  8. US
  9. 2025-09-17
  10. US
    Drugs & medicalClass II

    Lannett Company Inc. recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100 Tablets per…

    Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100ct, contained one (1) tablet of…

    FDA · DrugLannett Company Inc.OHOfficial notice →
  11. 2025-09-03
  12. US
    Drugs & medicalClass II

    Lannett Company Inc. recalls Lisdexamfetamine Dimesylate Capsules, 40 mg, 100-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136.…

    Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.

    FDA · DrugLannett Company Inc.Nationwide within the USAOfficial notice →
  13. 2024-12-11
  14. US
    Drugs & medicalClass II

    Lannett Company Inc. recalls Lisdexamfetamine Dimesylate Capsules, 10 mg, 100 Capsules per bottle, Rx only, Distributed by: Lannet Company, Philadelphia, PA 19136,…

    Failed Content Uniformity Specifications: Product failed to meet the action limits for stratified content uniformity.

    FDA · DrugLannett Company Inc.Nationwide in the USAOfficial notice →
  15. 2023-01-25
  16. US
  17. 2022-02-23
  18. US
    Drugs & medicalClass II

    Lannett Company, Inc. recalls Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed by: Lannett Company, Inc.,…

    Failed Impurities/Degradation Specifications: Out of specification results for related substances.

    FDA · DrugLannett Company, Inc.Product was distributed nationwide in the USA.Official notice →