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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

Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals: Products were not manufactured under cGMP's and were stored in uncontrolled temperature and humidity conditions.

Agency Publication Date: October 31, 2011
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 59089
Status: Resolved
Manufacturer: Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals
Manufactured In: United States
Units Affected: 21 products (644 bottles; 1,320 bottles; 238 bottles; 10 bottles; 3 bottles of 50 capsules; 4 bottles of tablets; 7 bottles of softgel capsules; 3 bottles of Capsulas; 4 bottles of capsulas; 3 bottles of Tabletas; 6 bottles of tabletas; 3 bottles of capsules; 603 Boxes of capsuls; 412 bottles of tablets; 99 boxes of tablets; 17,392 boxes of capsules; 3,354 Bottles; 225,412 PKGS; 411 boxes; 22 boxes; unknown)

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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.