Golden State Medical Recall: Atenolol Bottles Labeled Wrong
Golden State Medical Supply recalls Atenolol 25mg bottles due to a label mix-up containing Clopidogrel. Check your lot number GS046745.
Stop using this now
Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets
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What happened, in plain English
Golden State Medical Supply Inc. is recalling Atenolol Tablets, USP, 25 mg in 1000-count bottles because the labels were mixed up. A bottle labeled as Atenolol actually contained Clopidogrel 75mg tablets. This is a Class I recall, indicating a serious health risk. Read more at govinfonow.com/recall/34312-golden-state-medical-recall-atenolol-bottles-labeled-wrong.
Source Summary by GovInfoNow · govinfonow.com/recall/34312-golden-state-medical-recall-atenolol-bottles-labeled-wrong · Updated October 10, 2026 · FDA enforcement record: FDA #D-0019-2023
Cite this page
“Golden State Medical Recall: Atenolol Bottles Labeled Wrong.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/34312-golden-state-medical-recall-atenolol-bottles-labeled-wrong. Based on FDA recall #D-0019-2023 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0019-2023%22&limit=1).
Why it’s dangerous
The hazard is a label mix-up where a bottle intended to contain Atenolol (a beta-blocker) contained Clopidogrel (an antiplatelet agent). Taking Clopidogrel when expecting Atenolol can lead to serious adverse health effects or lack of necessary treatment.
Who’s affected
Patients who purchased or were prescribed the specific lot of Atenolol Tablets from Golden State Medical Supply are affected. Individuals relying on this medication for heart conditions are at immediate risk of taking the wrong drug.
How to tell if you have this one
Check if you have a 1000-count bottle of Atenolol Tablets, USP, 25 mg marketed by Golden State Medical Supply Inc. Look for NDC 60429-027-10 and Lot # GS046745 with an expiration date of 12/2023.
- Brand
Golden State Medical Supply- Category
Drug
What to do — step by step
Stop taking the medication
Do not consume any tablets from the recalled bottle immediately due to the risk of ingesting the wrong drug.
Contact your pharmacy or doctor
Reach out to your healthcare provider or pharmacist to discuss alternative treatment options and proper disposal.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “USA Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.5 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-0019-2023 (September 29, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0019-2023 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 10, 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.