Lannett Company Inc. 2024-12-11 Health serious FDA
Health · FDA · Recall #FDA-D-0112-2025
Lisdexamfetamine Dimesylate Capsules, 10 mg, 100 Capsules per bottle, Rx only,… Recall
Issued December 11, 2024 · Lannett Company Inc.
In December 2024, Lannett Company Inc. recalled the Lisdexamfetamine Dimesylate Capsules, 10 mg, 100 Capsules per bottle, Rx only,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed Content Uniformity Specifications: Product failed to meet the action limits for stratified content uniformity.
What you should do
- 1 Stop using Lisdexamfetamine Dimesylate Capsules, 10 mg, 100 Capsules per bottle, Rx only,… 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
- December 11, 2024
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0112-2025
- 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 737th Health recall we've logged in 2024.