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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

West Coast Laboratories Inc: West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).

Agency Publication Date: February 1, 2017
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Affected Products

Product: Xambo, 80 boxes of bulk capsules. Each containing 12,053 capsules in each box.

361215

Product: Devagrass

Lot No. CK15005 Mfg. Lot no. 620815

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 76003
Status: Resolved
Manufacturer: West Coast Laboratories Inc
Manufactured In: United States
Units Affected: 2 products (964,240 capsules; 3,600 blisters)

Were You Affected by This Recall?

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.

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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.