Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the Echinacea…
Recalling firm: Naturex Inc.
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 14, 2014.
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FDA code information
EC330955, Lot #C133/068/A13
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Full FDA record and distribution details
Original product description
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.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | C133/068/A13 | EC330955, Lot #C133/068/A13 |
Original FDA recall reason
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Recall details
- Recall number
- F-2177-2014
- Event ID
- 68530
- FDA status
- Terminated
- Initiated
- Jun 9, 2014
- Reported
- Jul 23, 2014
- Classified
- Jul 15, 2014
- Terminated
- Nov 14, 2014
- Quantity
- 9 boxes (25 kg each)
- Location
- S Hackensack, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
TN, TX, & WA
Data updated September 16, 2026. View official FDA data ↗
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