Golden State Medical Recalls Prasugrel HCl 10mg Tablets
Golden State Medical Supply recalls Prasugrel HCl 10mg tablets due to failed dissolution specifications. Check lot GS062298.
Use caution until it’s fixed
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
What happened, in plain English
Golden State Medical Supply Inc. is recalling one lot of Prasugrel HCl, Tablets, USP, 10mg because the product failed dissolution specifications. This means the tablets may not release the medication properly in the body. The recall affects 6,791 bottles distributed nationwide. Read more at govinfonow.com/recall/1004692-golden-state-medical-recalls-prasugrel-hcl-10mg-tablets.
Source Summary by GovInfoNow · govinfonow.com/recall/1004692-golden-state-medical-recalls-prasugrel-hcl-10mg-tablets · Updated October 9, 2026 · FDA enforcement record: FDA #D-0847-2026
Cite this page
“Golden State Medical Recalls Prasugrel HCl 10mg Tablets.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/1004692-golden-state-medical-recalls-prasugrel-hcl-10mg-tablets. Based on FDA recall #D-0847-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0847-2026%22&limit=1).
Why it’s dangerous
The hazard is that the tablets failed dissolution specifications, which can prevent the drug from being absorbed correctly. This could lead to reduced effectiveness of the medication for treating cardiovascular conditions.
Who’s affected
Patients who have been prescribed Prasugrel HCl 10mg tablets from this specific manufacturer and lot are affected. Individuals taking this medication may not receive the intended therapeutic effect due to the manufacturing defect.
How to tell if you have this one
Look for Prasugrel HCl, Tablets, USP, 10mg in a 30-count bottle marked with NDC: 51407-445-30. The specific recalled lot number is GS062298.
- Brand
Golden State Medical Supply- Category
Drug
What to do — step by step
Contact Your Pharmacist
Reach out to your pharmacy or healthcare provider immediately to discuss the recall and obtain a replacement if necessary.
Verify Lot Number
Check your medication bottle for lot number GS062298 to confirm if it is part of this specific recall.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 19 days after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class II
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
Questions people ask
Where was this product sold?
The product was distributed nationwide in the United States.
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Where this comes from
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.
- Official source: FDA Recall #D-0847-2026 (August 21, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0847-2026 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.