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.

Read the official notice →
Date
2025-09-03
Country
United States
Brand
Lannett
Product
Lisdexamfetamine Dimesylate Capsules, 40 mg, 100-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136.…
Classification
Class II
Units
Nationwide within the USA
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Lannett recalls

  1. 2026-05-27
  2. 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 →
  3. 2025-10-29
  4. US
  5. 2025-09-17
  6. 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 →
  7. 2024-12-11
  8. 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 →
  9. 2023-01-25
  10. US
  11. 2022-02-23
  12. 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 →
All 9 Lannett recalls →

Other drugs & medical recalls in the United States

  1. 2025-09-03
  2. US
    Drugs & medicalClass I

    Tandem Diabetes Care, Inc. recalls Battery Operated infusion pumps. t:slim X2 G5, Replacement, Refurbished, REF: 1000911; t:slim X2 GS Classic, Replacement, Refurbished,…

    Insulin pumps manufactured with speakers from Revision A and B may malfunction ("Malfunction 16") which prevents audible alerts and causes the pumps to become inoperable and stop infusing insulin which could result in…

    FDA · DeviceTandem Diabetes Care, Inc.Worldwide distribution. US nationwide including Puerto Rico, Canada, Czech…Official notice →
  3. US
    Drugs & medicalClass II

    GE Medical Systems, LLC recalls GE HealthCare OEC 9900 Elite C-arm Systems.

    GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator…

    FDA · DeviceGE Medical Systems, LLCUS Nationwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue, Conshohocken, PA 19428,…

    Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

    FDA · DrugMEDLINE INDUSTRIES, LP - NorthfieldNationwideOfficial notice →
  5. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217…

    CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity…

    FDA · DrugAmerisource Health Services LLCNationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    Cardinal Health Inc. recalls Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL, packaged in 0.3 mL prefilled syringes further packaged in bags of 5 prefilled syringes, Rx…

    Correct Labeled Product Mispack: Bags labeled for Enoxaparin Sodium Injection, 80 mg/0.8 mL, contained Enoxaparin Sodium Injection, 30 mg/0.3 mL

    FDA · DrugCardinal Health Inc.KSOfficial notice →
  7. US
See all drugs & medical recalls →