Golden State Medical Supply Inc. is recalling 108 bottles of Budesonide (budesonide) Extended-Release Tablets, 9 mg, in 30-count bottles. The recall was initiated because the tablets failed dissolution testing, which measures how the medication dissolves and is released into the body. No incidents or injuries have been reported to date. This drug is an Rx-only medication marketed by GSMS, Incorporated and was distributed only in Illinois.
The tablets failed dissolution specifications, meaning the medication may not release properly in the digestive tract. This can result in sub-therapeutic levels of the drug, making the treatment ineffective, or potentially causing the drug to be released too quickly, increasing the risk of side effects.
You have 2 options:
Rx only; Marketed by GSMS, Incorporated, Camarillo, CA.
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.