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.

Check the codes ↓

The exact 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.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

ED161322, Lot #C129/081/A13

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 ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.