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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 Food

Naturex Inc.: Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.

Agency Publication Date: July 15, 2014
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Affected Products

Product: Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg.

EC330955, Lot #C133/068/A13

Lot Numbers:
C133
Product: Echinacea Agustifolia PE 4& echinosides The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg.

ED161322, Lot #C129/081/A13

Lot Numbers:
C129
Product: Echinacea Angustifolia Root PE 4: The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg.

EC330955, Lot#C073/050/A14

Lot Numbers:
C073

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 68530
Status: Resolved
Manufacturer: Naturex Inc.
Manufactured In: United States
Units Affected: 3 products (9 boxes (25 kg each); 4 boxes (each 25 kg); 25 kg)

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.