FDA Food recall F-2177-2014
Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard bo…
- FDA Food
- Class III
- terminated
- Published 2014-07-23
On 2014-07-23 the FDA classified a Class III recall of Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard bo… by Naturex, citing products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-2177-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-06-09 |
| Published | 2014-07-23 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | Naturex |
| Distribution | TN, TX, WA |
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.
Reason
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Identifiers
| code_info | EC330955, Lot #C133/068/A13 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2177-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.