FDAFDA · Food and drugs·Recall number F-2179-2014
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.
Published July 23, 2014 · Recall initiated: June 9, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Naturex Inc.
- Distributor
- TN, TX, & WA
- Lot
- EC330955, Lot#C073/050/A14
- Risk classification
- Class III
- Area (FDA)
- food
- Country
- United States
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