Why it was recalled
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Product description
Echinacea Angustifolia Root PE 4: 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#C073/050/A14
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-2179-2014
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Jun 9, 2014
- FDA report date
- Jul 23, 2014
- Quantity
- 25 kg
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Naturex Inc.
Original FDA data
Every field from FDA enforcement report F-2179-2014, 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#C073/050/A14
- Postal code
- 07606-1532
- Report date
- Jul 23, 2014
- Product type
- Food
- Recall number
- F-2179-2014
- Classification
- Class III
- Recalling firm
- Naturex Inc.
- Product quantity
- 25 kg
- 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 Angustifolia Root PE 4: 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