Golden State Medical Supply Inc. recalls Losartan Potassium Tablets, USP, 25 mg, Rx only, a) 30 ct. (NDC 60429-316-30) b) 90ct. (NDC 60429-316-90) c) 1,000 ct.
Golden State Medical Supply recalls 25mg Losartan Potassium Tablets (NDC 60429-316-30, 90ct, 1000ct) due to impurity detected in active ingredient. Consumers should contact the company for details.
Recall notice
CGMP Deviations: Impurity for N-nitroso-N-methyl-4-aminobutryric Acid (NBMA) detected in active ingredient (API) used to manufacture finished products.
Contact the company & request your remedy
What happened, in plain English
Golden State Medical Supply is recalling 25mg Losartan Potassium Tablets because impurities were found in the active ingredient. This could pose a health risk to people taking the medication. Read more at govinfonow.com/recall/37202-golden-state-medical-supply-recalls-25mg-losartan-potassium-tablets-due.
Source Summary by GovInfoNow · govinfonow.com/recall/37202-golden-state-medical-supply-recalls-25mg-losartan-potassium-tablets-due · Updated October 5, 2026 · FDA enforcement record: FDA #D-1238-2020
Cite this page
“Golden State Medical Supply recalls 25mg Losartan Potassium Tablets due to impurity risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37202-golden-state-medical-supply-recalls-25mg-losartan-potassium-tablets-due. Based on FDA recall #D-1238-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1238-2020%22&limit=1).
Why it’s dangerous
The recall is due to the detection of an impurity called N-nitroso-N-methyl-4-aminobutryric Acid in the active ingredient used to make the tablets. This impurity could potentially cause health issues when taken by patients.
Who’s affected
People who have been prescribed this medication by a doctor. Those taking the medication for high blood pressure or other conditions are most at risk.
How to tell if you have this one
Check for the product name 'Losartan Potassium Tablets, USP, 25 mg, Rx only' with the NDC codes 60429-316-30, 60429-316-90, or 60429-316-10. The product was manufactured by Arrow Pharm (Malta) Ltd. and packaged by Golden State Medical Supply.
- Brand
Golden State Medical Supply- Category
Drug
What to do — step by step
Contact Manufacturer
Reach out to Golden State Medical Supply for specific instructions on how to handle the recalled product.
Questions people ask
Is this product safe to take?
The recall indicates an impurity was detected in the active ingredient, so it is not safe to take without consulting the manufacturer first.
What should I do if I have this product?
Contact Golden State Medical Supply for specific instructions on how to handle the recalled product.
How can I check if I have the recalled product?
Look for the product name 'Losartan Potassium Tablets, USP, 25 mg, Rx only' with the NDC codes 60429-316-30, 60429-316-90, or 60429-316-10.
Contact Golden State Medical Supply
We’ve drafted a message you can send Golden State Medical Supply to request your refund or repair — edit it as you like.
Subject: Recall D-1238-2020 — Golden State Medical Supply Golden State Medical Supply Hello, I own a Golden State Medical Supply that is covered by recall D-1238-2020 from Golden State Medical Supply. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-1238-2020 (April 3, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1238-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.