A widely used ADHD medication has been recalled nationwide after failing important quality checks. The recall involves several strengths of generic lisdexamfetamine, a stimulant used to treat ADHD and binge eating disorder. Lab tests showed the capsules did not dissolve correctly, which means the medicine may not work the way it should.
The FDA labeled this a Class II recall, meaning the issue could cause temporary or reversible health problems. Dozens of lots are affected, with expiration dates between February and May 2026. The recalled products range from 10 mg to 70 mg. Patients can check their bottles by matching the lot number on the packaging.
No symptoms or injuries have been reported, and officials have not issued specific instructions for patients. Anyone who has the recalled medication should contact their pharmacist or doctor to find out what to do next. The recall highlights how important proper drug dissolution is, because even small changes can affect how a medication is absorbed and how well it works.
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