Echinacea Agustifolia Root PE 4
Reason Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Echinacea Agustifolia PE 4& echinosides The product is in powder… recall
Recalled by Naturex Inc. · S Hackensack, NJ, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Echinacea Agustifolia PE 4& echinosides The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg.
Quantity: 4 boxes (each 25 kg)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
ED161322, Lot #C129/081/A13
Where it was sold
Tennessee Texas Washington
FDA's distribution note: TN, TX, & WA
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Naturex Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 9, 2014
- In FDA report of
- Jul 23, 2014
- Terminated
- Nov 14, 2014
- FDA recall number
- F-2178-2014 · event 68530
- Official record
- FDA enforcement report search
Also recalled with it (2 more products)
FDA files each product of one recall action separately; these share the same FDA event.
Echinacea Angustifolia Root PE 4
Reason Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Other recalls by Naturex Inc.
Dried Brewers Yeast TG_YFS004 Naturex 375 Huyler Street
Reason The affected lots were tested and found to contain an unusual high level of selenium.