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.
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 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg.
Lannett is recalling 10mg ADHD medication tablets that contain an extra 5mg tablet. This foreign tablet could cause incorrect dosing if taken, potentially leading to unsafe medication levels.
The recalled tablets contain an extra 5mg tablet that wasn't supposed to be there. This could lead to taking too much medication, causing side effects like increased heart rate or anxiety.
People who own or use the recalled 10mg ADHD medication tablets. Those who take the medication as prescribed are most at risk of incorrect dosing.
Check for bottles labeled as 10mg ADHD medication with 100 tablets. Look for the lot number 25283185A and expiration date 02/28/2027 on the packaging.
Look for the lot number 25283185A and expiration date 02/28/2027 on the packaging.
The recall is for foreign tablets that could cause incorrect dosing, but the medication itself is safe when used correctly.
Check for bottles labeled as 10mg ADHD medication with 100 tablets, lot number 25283185A, and expiration date 02/28/2027.
No immediate action is needed, but verify the product details to ensure you have the correct medication.
We’ve drafted a message you can send Lannett to request your refund or repair — edit it as you like.
Subject: Recall D-0642-2025 — Lannett Lannett Hello, I own a Lannett that is covered by recall D-0642-2025 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.
