Iowa Select Herbs LLC recalls echinacea supplements due to misbranding, unapproved status, and adulteration. Consumers should check product labels for lot numbers and expiration dates.
Pursuant to a consent decree for injunctive relief the recalling firm was ordered to recall all products because they are misbranded, unapproved new drugs and adulterated dietary supplements.
Iowa Select Herbs is recalling echinacea supplements because they are misbranded, unapproved as new drugs, and adulterated dietary supplements. This recall is required by a court order to address illegal product claims.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (containing harmful substances). This makes them unsafe for consumption as dietary supplements.
Anyone who purchased Iowa Select Herbs echinacea products with lot numbers from 32263 (expiring April 2020) is affected. People using these products for medicinal purposes are at higher risk due to the unapproved status.
Check for the brand 'Iowa Select Herbs' and product names like Echinacea Purpurea. Look for lot number 32263 and expiration date of April 2020 on the label.
Look for the lot number 32263 and expiration date of April 2020 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as required by a court order.
Check the product label for lot number 32263 and expiration date of April 2020. If it matches, stop using it and contact the manufacturer.
The recall notice does not specify a return deadline.
We’ve drafted a message you can send Iowa Select Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-1171-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1171-2016 from Iowa Select Herbs. 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.
