Class IIITerminated in FDA datasetJun 9, 2014

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.

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 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.

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

EC330955, Lot #C133/068/A13

TypeCode / valueContext
lotC133/068/A13EC330955, Lot #C133/068/A13

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

FDA source record · F-2177-2014

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.