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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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Low RiskFDA Drug

Lex, Inc.: Misbranding: Non-compliance with FDA requirements OTC labeling and monograph requirements

Agency Publication Date: September 30, 2005
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 33415
Status: Resolved
Manufacturer: Lex, Inc.
Manufactured In: United States
Units Affected: 7 products (528 cases; 2122 cases; 1155 cases; 3175 cases; 4237 cases; 3770 cases; 10695 cases)

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 · 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.