Class IIITerminated in FDA datasetJun 9, 2014

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.

Recalling firm: Naturex Inc.

Why it was recalled

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

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ProductEchinacea 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.

FDA code information

ED161322, Lot #C129/081/A13

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Full FDA record and distribution details

Original product description

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.

Extracted codes and context

TypeCode / valueContext
lotC129/081/A13ED161322, Lot #C129/081/A13

Recall details

Recall number
F-2178-2014
Event ID
68530
FDA status
Terminated
Initiated
Jun 9, 2014
Reported
Jul 23, 2014
Classified
Jul 15, 2014
Terminated
Nov 14, 2014
Quantity
4 boxes (each 25 kg)
Location
S Hackensack, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

TN, TX, & WA

FDA source record · F-2178-2014

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.