FDA recall record
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.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 14, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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.
Reason
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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.
Code information listed by FDA
EC330955, Lot#C073/050/A14
Distribution and firm information
Recalling firm listed by FDA: Naturex Inc.
Firm location listed by FDA: S Hackensack, NJ, United States
Distribution reported by FDA: TN, TX, & WA
Product quantity listed by FDA: 25 kg
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.