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Naturex Inc.
FDA recall F-2178-2014 · Class III · reported 2014-07-23 · Terminated
- 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.
- Reason
- Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
- Quantity
- 4 boxes (each 25 kg)
- Distribution
- TN, TX, & WA
- Firm location
- NJ, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Telephone
- Recall started
- 2014-06-09
- Terminated
- 2014-11-14
- Code info
- ED161322, Lot #C129/081/A13
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.