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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Golden State Medical Supply Inc.: Omeprazole Delayed Release Capsules Recalled for Failed Impurity Specifications

Agency Publication Date: March 24, 2021
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Summary

Golden State Medical Supply Inc. has voluntarily recalled one lot of Omeprazole Delayed Release Capsules (20 mg, 1000-count bottles). This prescription medication, used to treat frequent heartburn and stomach acid issues, was found to contain unknown impurities that exceeded safety specifications during stability testing. Consumers should contact their healthcare provider or pharmacist regarding this recall, as the presence of unauthorized degradation products or impurities can affect the safety and effectiveness of the medication. This specific lot was distributed to wholesalers under government contracts in Pennsylvania and Texas.

Risk

The drug failed stability testing because it contained unknown impurities or degradation products above the permitted levels. These impurities can potentially cause unexpected side effects or reduce the medication's ability to treat the intended condition.

What You Should Do

  1. Check your prescription bottle for Omeprazole Delayed Release Capsules, USP, 20 mg, in 1000-count bottles with NDC 51407-129-10.
  2. Verify if your bottle matches Lot Number GS029673 with an Expiration Date of 5/2021.
  3. Contact your healthcare provider or pharmacist immediately for guidance if you are taking medication from the affected lot.
  4. Return any unused capsules from the affected lot to your pharmacy for a refund.
  5. Contact the manufacturer, Golden State Medical Supply Inc., at their Camarillo, CA location for further instructions regarding the return of the product.
  6. For additional questions or to report a problem, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund
How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund.

Affected Products

Product: Omeprazole Delayed Release Capsules, USP, 20 mg (1000-count bottle)
Model:
NDC 51407-129-10
Recall #: D-0312-2021
Lot Numbers:
GS029673 (Exp. Date 5/2021)
Date Ranges: Expiration Date 5/2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87566
Status: Resolved
Manufacturer: Golden State Medical Supply Inc.
Sold By: Wholesalers/distributors under government contract
Manufactured In: United States
Distributed To: Pennsylvania, Texas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.