Golden State PRASUGREL Tablets 5mg Recall: Failed Dissolution Specifications
Golden State Medical Supply recalls 5mg PRASUGREL tablets with failed dissolution specs. Check NDC 51407-444-30 and specific lot numbers for affected products.
Lower-risk recall
Failed Dissolution Specifications
Contact the company
What happened, in plain English
Golden State Medical Supply is recalling 5mg PRASUGREL tablets that failed dissolution specifications. This means the tablets may not work as intended when taken, which could affect blood thinning effectiveness. Read more at govinfonow.com/recall/32247-golden-state-prasugrel-tablets-5mg-recall-failed-dissolution-specifications.
Source Summary by GovInfoNow · govinfonow.com/recall/32247-golden-state-prasugrel-tablets-5mg-recall-failed-dissolution-specifications · Updated August 17, 2026 · FDA enforcement record: FDA #D-0287-2025
Cite this page
“Golden State PRASUGREL Tablets 5mg Recall: Failed Dissolution Specifications.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32247-golden-state-prasugrel-tablets-5mg-recall-failed-dissolution-specifications. Based on FDA recall #D-0287-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0287-2025%22&limit=1).
Why it’s dangerous
The tablets failed dissolution specifications, meaning they may not release the active ingredient properly in the body. This could lead to ineffective blood thinning, increasing the risk of blood clots.
Who’s affected
Prescription holders of the recalled 5mg PRASUGREL tablets. Patients taking blood thinners for heart conditions are most at risk.
How to tell if you have this one
Check for NDC 51407-444-30 on the packaging. Affected lots include GS059908, GS060228, GS060709, GS061233, GS061704, GS062158, GS062405, expiring April 30, 2026.
- Brand
Golden State Medical Supply- Category
Drug
What to do — step by step
Check Product Details
Look for NDC 51407-444-30 and specific lot numbers on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “U.S. 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 21 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have the recalled product?
Check the product details and lot numbers to see if it's affected. If it is, contact your doctor for alternative options.
Similar recalls
Other Golden State Medical Supply recalls
Latest drug recalls
Keep exploring
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-0287-2025 (March 5, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0287-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 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.