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.
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.
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.
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.