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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

keen-wah LLC: An anti-stick spray containing soy lecithin was used during the manufacture of several varieties of i heart keenwah, quinoa clusters and soy was not declared on the product labeling.

Agency Publication Date: April 4, 2014
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Affected Products

Product: i heart keenwah Chocolate Sea Salt All Natural Quinoa Clusters. UPC 736211802446 for the 4 oz UPC 713757598101 for the 1 oz

All codes which read EXPDDMMYY (all dates)

Product: i heart keenwah Almond All Natural Quinoa Clusters. UPC 736211802347 for the 4 oz UPC 713757598200 for the 1 oz

All codes which read EXPDDMMYY (all dates)

Product: i heart keenwah Ginger Peanut All Natural Quinoa Clusters. UPC 736211802644 for the 4 oz UPC 713757598408 for the 1 oz

All codes which read EXPDDMMYY (all dates)

Product: i heart keenwah Cranberry Cashew All Natural Quinoa Clusters. UPC 736211802545 for the 4 oz UPC 713757598309 for the 1 oz

All codes which read EXPDDMMYY (all dates)

Product: i heart keenwah Peanut Butter Cacao All Natural Quinoa Clusters. UPC 736211884442 - 4 oz 12 units/cs

All codes which read EXPDDMMYY (all dates)

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 67848
Status: Resolved
Manufacturer: keen-wah LLC
Manufactured In: United States
Units Affected: 5 products (Approximately 8032 cs 4 oz 12 units/cs; 1 oz 24 units/cs; approximately 4899 cs - 4 oz 12 units/case; approximately 475 cs - 1 oz 24 units/cs; approximately 3143 cs - 4 oz 12 units/case; approximately 322 cs - 1 oz 24 units/cs; approximately 4979 cs -4 oz 12 units/cs; approximately 511 cs -1 oz 24 units/cs; approximately 1405 cs - 4 oz packages/12 per case)

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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.