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.

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

Recall #: F-2178-2014
Affected scope: 4 boxes (each 25 kg)
Initiated: June 9, 2014

Compiled from official public sources by the publisher. · Updated September 2026

Naturex Inc. recalled Echinacea Agustifolia PE 4& echinosides The product is in powder form extracted from t… - a low-severity action.

Echinacea Agustifolia PE 4& echinosides The product is in powder form extracted from t… was recalled by Naturex Inc. in July 23, 2014. Reason: Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.. Check the official notice for the remedy. Verify recall #F-2178-2014 with the FDA Food before acting.

The recall

Naturex Inc. issued this low-severity FDA Food recall-Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507..

Low
severity level: Class III
classification: July 23, 2014
reported

Sourced from official FDA Food enforcement records. Verify recall #F-2178-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

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.

Reason for recall

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

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Low (Class III)
Status	Terminated
Recall number	F-2178-2014
Date reported	July 23, 2014
Date initiated	June 9, 2014
Recalling firm	Naturex Inc.
Firm location	S Hackensack, NJ
Affected scope	4 boxes (each 25 kg)
Distribution	TN, TX, & WA

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-2178-2014) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

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.. Recalled by Naturex Inc.. Units affected: 4 boxes (each 25 kg).

Why was this product recalled? ▼

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

Which agency issued this recall? ▼

This recall was issued by the FDA Food on July 23, 2014. Severity: Low. Recall number: F-2178-2014.

Where was the recalled product distributed? ▼

Distribution: TN, TX, & WA.

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Low), closest by report date among other firms and states.

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Similar Food · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported July 23, 2014. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026