11/10/2025
The FDA has recalled certain batches of the GENERIC form of Vyvanse (Lisdexamfetamine Dimesylate) due to poor dissolution of the affected capsules. This means the capsule may not deliver the optimal amount of medication, potentially impacting its therapeutic effectiveness.
The recall applies only to capsules manufactured by Sun Pharmaceutical Industries.
You can verify whether your prescription is affected by checking your medication bottle for the manufacturer’s name or by contacting your pharmacy.
See the link below for a list of the affected prescription bottle specifications and lot numbers.
https://www.pharmacy.ca.gov/about/recall_alerts/103125_sun.pdf
https://www.11alive.com/article/news/nation-world/adhd-medication-recall-failed-tests/507-b7c9a9e8-36bc-488b-94f2-4613d84105ca
If you need a new prescription please send your request via our portal system.