Naturex recalls Echinacea Agustifolia powder due to azoxystrobin contamination, a pesticide with no allowed tolerance in food. Consumers should check product labels for ED161322 lot numbers.
Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.
Naturex is recalling Echin: Agustifolia powder because it contains azoxystrobin, a pesticide that is not permitted in food products. This could pose a health risk if consumed.
The powder contains azoxystrobin, a pesticide that is not allowed in food products according to U.S. federal regulations. This chemical is present in the product despite being prohibited for use in food, which could lead to unintended consumption.
People who purchased the Echinacea Agustifolia powder from Naturex, typically those using herbal supplements for immune support. Those with sensitive health conditions or allergies to pesticides may be at higher risk.
Check for the product name 'Echinacea Agustifolia PE 4& echinosides' on the label. Look for lot numbers ED161322 and C129/081/A13 on the packaging.
Look for the product name 'Echinacea Agustifolia PE 4& echinosides' and lot numbers ED161322 or C129/081/A13 on the packaging.
The recall states the product contains azoxystrobin, a pesticide not permitted in food, but no specific safety instructions are provided beyond checking the label.
Check for the product name 'Echinacea Agustifolia PE 4& echinosides' and lot numbers ED161322 or C129/081/A13 on the packaging.
The recall does not specify a remedy, so the official notice only advises checking the label for the product name and lot numbers.
We’ve drafted a message you can send Naturex to request your refund or repair — edit it as you like.
Subject: Recall F-2178-2014 — Naturex Naturex Hello, I own a Naturex that is covered by recall F-2178-2014 from Naturex. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
