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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 Food

Kirkman Group Inc., DBA Kirkman Laboratories Inc.: products contain undeclared antimony

Agency Publication Date: April 27, 2010
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 54185
Status: Resolved
Manufacturer: Kirkman Group Inc., DBA Kirkman Laboratories Inc.
Manufactured In: United States
Units Affected: 7 products (11133 bottles (includes all container sizes); 2319 bottles (all bottle sizes); 405 tubs (7 oz each); 157 tubs; 216 bottles; 146 16oz containers and 83 trial size containers; 604 tubs (includes all sizes))

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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.