Lannett Company Inc. recalls
Every recall we track for Lannett Company Inc. — 15 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
15 recalls since 2017.
All FDA recall records for Lannett Company Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 1 | 1 |
| 2019 | 0 | 0 | 1 | 2 | 3 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 1 | 2 | 3 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 0 | 2 | 1 | 3 |
| 2026 (to date) | 0 | 0 | 3 | 0 | 3 |
Most common reasons for Lannett Company Inc. recalls
What to do if you have a recalled Lannett Company Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Lannett Company Inc. recalls
14 shown- Lower riskDrug
Lannett Company Inc. recalls Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Lannett Company recalls 5mg extended-release dextroamphetamine capsules due to labeling error. Capsules contain only immediate-release pellets but are labeled as extended-release. No immediate action needed but check labels carefully.
Lann: A short, human brand name for headings (e.g.Jun 26, 2026 - Lower riskDrug
Lannett Company Inc. recalls Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett Company, Inc.,
Lannett recalls 1,000 mg niacin extended-release tablets due to failed dissolution testing. This may affect medication effectiveness. Contact Lannett for details.
LannettMay 27, 2026 - Lower riskDrug
Lannett Company Inc. recalls Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136,
Lannett recalls Primidone 250mg tablets due to trace acemetacin contamination. Affected lots have specific expiration dates and are prescription-only.
LannettApr 24, 2026 - UnratedDrug
Lannett Company Inc. recalls Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distributed by: Lannett Company, Inc.,
Lannett Company recalls 1,000 mg niacin extended-release tablets (Rx only) due to failed dissolution specifications. This may affect safety in normal use. Check NDC and lot numbers for affected batches.
LannettOct 10, 2025 - Lower riskDrug
Lannett Company Inc. recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg,
Lannett recalls 10mg ADHD medication bottles with foreign tablets. Consumers should check for 5mg tablets in 100-count bottles. No immediate action needed but verify product details.
LannettAug 19, 2025 - Lower riskDrug
Lannett Company Inc. recalls Lisdexamfetamine Dimesylate Capsules, 40 mg, 100-count bottles, Rx Only, Distributed by: Lannett Company, Inc.,
Lannett recalls 40mg Lisdexamfetamine capsules due to label mix-up with 30mg strength. This could lead to incorrect dosing if taken without proper label check.
LannettAug 11, 2025 - Lower riskDrug
Lannett Company Inc. recalls Lisdexamfetamine Dimesylate Capsules, 10 mg, 100 Capsules per bottle, Rx only, Distributed by: Lannet Company,
Lannett recalls 10mg Lisdexamfetamine Dimesylate capsules due to failed content uniformity. This affects Rx-only products with specific NDC and lot numbers. Consumers should contact the manufacturer for details.
LannettOct 25, 2024 - UnratedDrug
Lannett Company Inc. recalls Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle,
Lannett recalls triamterene and hydrochlorothiazide capsules (37.5 mg/25 mg) due to failed impurity and degradation specifications. Rx-only capsules with NDC 0527-1632-01 or 0527-1632-10 lots 21000279A (exp 01/2023) and 20256320A (12/2022) are affected.
LannettNov 9, 2022 - Lower riskDrug
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 recalls Diazepam Oral Solution bottles with specific lot numbers due to impurities that may cause harm. Consumers should contact the manufacturer for details.
LannettFeb 9, 2022 - Lower riskDrug
Lannett Company, Inc. recalls Prednisone Tablets, USP 2.5 mg, 100 tablets, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136,
Lannett recalls 2.5mg prednisone tablets that were mislabeled as 10mg. This could lead to incorrect dosing. Check your bottle's label and contact Lannett for details.
LannettAug 10, 2020 - UnratedDrug
Lannett Company, Inc. recalls Levetiracetam Oral Solution 100mg/mL, 473 mL (16 fl. oz.) Bottles, Rx Only, Distributed by: Lannett Company, Inc.
Lannett recalls Levetiracetam Oral Solution 100mg/mL bottles due to microbial contamination. This medication is prescription-only and may pose health risks if used without proper sterility.
LannettDec 6, 2019 - UnratedDrug
Lannett Company, Inc. recalls Lannett Ranitidine Syrup (Ranitidine Oral Solution, USP), 15mg/mL Rx Only Distributed by: Lannett Company, Inc.
Lannett Company recalls ranitidine syrup due to detected NDMA impurity. This may pose health risks. Check your product's NDC codes for affected batches.
LannettOct 28, 2019 - Lower riskDrug
Lannett Company Inc. recalls Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc,
Lannett recalls 10mg Oxybutynin Extended-Release Tablets (NDC 62175-271-37) due to failed dissolution specifications. Rx-only medication with specific batch numbers and expiration dates.
LannettFeb 21, 2019 - UnratedDrug
Lannett Company, Inc. recalls HydrOXYzine HYDROCHLORIDE SYRUP (HydrOXYzine Hydrochloride Oral Solution, USP), 10 mg per 5 mL, Rx only, Distributed by
Lannett recalls HydrOXYzine Hydrochloride Syrup (10mg/5mL) due to manufacturing impurities. Rx-only product distributed by Lannett Company Inc. in the US. No remedy specified in recall notice.
LannettOct 11, 2018
Lannett Company Inc. recall questions
How many recalls has Lannett Company Inc. had?
15 recalls from Lannett Company Inc. are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Lannett Company Inc. recall?
Lannett Company Inc. recalls Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, dated Jun 26, 2026. Every Lannett Company Inc. recall is listed on this page, newest first.
Why are Lannett Company Inc. products recalled?
The most common reasons on record: Failed Dissolution Specifications (2); Failed Impurity/Degradation Specifications (2).
What should I do if I have a recalled Lannett Company Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Lannett Company Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.