Echinacea Angustifolia Root PE (Naturex Inc.) – pesticide tolerance (2014)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Naturex Inc.
Lot Codes / Batch Numbers
EC330955, Lot#C073/050/A14
Products Sold
EC330955, Lot#C073/050/A14
Naturex Inc. is recalling Echinacea Angustifolia Root PE 4: The product is in powder form extracted from the Echinacea root p due to Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
TN, TX, WA
Page updated: Jan 6, 2026