Echinacea Angustifolia Root PE 4: The product is in powder form… — Class III food recall F-2179-2014
Terminated recall by Naturex Inc., reported 2014-07-23, distributed in TN, TX, WA. Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
| Recall number | F-2179-2014 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Naturex Inc., S Hackensack, NJ, United States |
| Recall initiated | 2014-06-09 |
| Classified | 2014-07-15 |
| Reported by FDA | 2014-07-23 |
| Terminated | 2014-11-14 |
| Distributed | TN, TX, WA |
| Quantity | 25 kilograms |
| Lot numbers | C073/050/A14 |
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.
Reason for recall
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-2179-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.