Class IIDrug
Prasugrel HCI recall
Summary
Golden State Medical Supply Inc. is recalling Prasugrel HCI (drug). According to the FDA report, the reason is: Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution. The FDA rated this a Class II: the product may cause temporary or medically reversible health problems; serious harm is unlikely. Recall status: Ongoing.
Details from the FDA report
- Product
- Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC: 51407-445-30.
- Reason
- Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
- Lot / code info
- Lot # GS062298, Exp Date: 09/30/ 2026.
- Quantity
- 6791 30-count bottles
- Distribution
- US Nationwide.
- Recalling company
- Golden State Medical Supply Inc., Camarillo, CA United States
- Recall started
- August 21, 2026
- FDA report date
- September 9, 2026
- Classification
- Class II: The product may cause temporary or medically reversible health problems; serious harm is unlikely.
- Voluntary / mandated
- Voluntary: Firm initiated
- Status
- Ongoing
- Recall number
- D-0847-2026
What to do
- Check whether you have this product, and compare the lot numbers, codes, or dates on your package with the codes listed above.
- If it matches, stop using it and keep it away from children and pets.
- Contact the recalling company (Golden State Medical Supply Inc.) or the store where you bought it about returns or refunds.
- Do not stop a prescribed medication without first talking to your pharmacist or doctor; they can help find a safe replacement.
- If you think the product made you or someone else sick, contact a doctor or pharmacist. In an emergency call 911.
- You can report problems to the FDA via MedWatch.