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Class III: unlikely to cause harmTerminated

Naturex Echinacea Agustifolia Root PE 4:1 The Recall

Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the E…

Naturex Inc. · S Hackensack, NJ

Risk level
Class III
Reported by FDA
Jul 23, 2014
Recall ID
F-2177-2014
Check your lot numberHow we source this data

Summary

Naturex recalled Echinacea Agustifolia Root PE 4:1 The starting Jun 9, 2014. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-2177-2014 on Jul 23, 2014. Reason: Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507. Status: Terminated.

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

EC330955, Lot #C133/068/A13

Where it was sold

TN, TX, & WA

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2177-2014
Classification
Class III
Status
Terminated
Recall initiated
Jun 9, 2014
FDA report date
Jul 23, 2014
Quantity
9 boxes (25 kg each)
Recall type
Voluntary: Firm initiated
Recalling firm
Naturex Inc.

Original FDA data

Every field from FDA enforcement report F-2177-2014, exactly as published.

Show all FDA fields
City
S Hackensack
State
NJ
Status
Terminated
Country
United States
Event ID
68530
Address
375 Huyler St
Code information
EC330955, Lot #C133/068/A13
Postal code
07606-1532
Report date
Jul 23, 2014
Product type
Food
Recall number
F-2177-2014
Classification
Class III
Recalling firm
Naturex Inc.
Product quantity
9 boxes (25 kg each)
Termination date
Nov 14, 2014
Reason for recall
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
TN, TX, & WA
Recall initiation date
Jun 9, 2014
Initial firm notification
Telephone
Center classification date
Jul 15, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2177-2014, published Jul 23, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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