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.
Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.
Lannett is recalling 40mg Lisdexamfetamine Dimesylate capsules because some bottles were mislabeled as 40mg but contain 30mg. This mix-up could cause incorrect dosing if users take the capsules without checking the label.
The capsules were mislabeled as 40mg but actually contain 30mg. This could lead to incorrect dosing if users take the capsules without checking the label, potentially causing underdosing or overdosing depending on the intended dose.
People who have the 40mg Lisdexamfetamine capsules with the NDC 0527-4664-37 lot number 25280726A. Those taking the medication for ADHD or binge eating disorder are most at risk of incorrect dosing.
Check for the NDC code 0527-4664-37 and lot number 25280726A on the bottle. The product is a 100-count bottle of Lisdexamfetamine Dimesylate Capsules, 40mg, Rx Only.
Verify the label on the bottle to ensure it correctly states 40mg Lisdexamfetamine Dimesylate Capsules.
The product was mislabeled as 40mg but contains 30mg Lisdexamfetamine Dimesylate Capsules, which could lead to incorrect dosing.
Look for the NDC code 0527-4664-37 and lot number 25280726A on the bottle, which is a 100-count bottle of Lisdexamfetamine Dimesylate Capsules, 40mg, Rx Only.
Check the label to ensure it correctly states 40mg. If it shows 30mg, contact your healthcare provider for guidance.
We’ve drafted a message you can send Lannett to request your refund or repair — edit it as you like.
Subject: Recall D-0599-2025 — Lannett Lannett Hello, I own a Lannett that is covered by recall D-0599-2025 from Lannett. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
