Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx… was recalled on August 21, 2026 in cooperation with the U.S. Food and Drug Administration because failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution.
Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC: 51407-445-30.
Lot # GS062298, Exp Date: 09/30/ 2026.
Units affected: 6791 30-count bottles
Where it was sold: US Nationwide.
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Golden State Medical Supply Inc.
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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