Iowa Select Herbs LLC recalls kava kava root products due to misbranding, unapproved status, and adulteration as dietary supplements. 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 kava kava root supplements because they are misbranded, unapproved new drugs, and adulterated dietary supplements. This recall is required by a consent decree to address legal violations.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated dietary supplements (containing harmful substances). This violates federal laws and poses potential health risks.
Anyone who purchased Iowa Select Herbs kava kava root products with lot numbers 30540 or 33660, expiring February 2020, is affected. People using these products for dietary supplements are most at risk due to the legal violations.
Check for lot numbers 30540 or 33660 on the product label, which expire February 2020. Products sold online at www.iowaselectherbs.com are included in this recall.
Look for lot numbers 30540 or 33660 on the product label, which expire February 2020.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as required by a consent decree for injunctive relief.
Check the product label for lot numbers 30540 or 33660 expiring February 2020. If you have these products, contact Iowa Select Herbs LLC for guidance.
The products are unapproved new drugs and adulterated, which could pose health risks, but the recall is required by legal action, not an immediate safety hazard.
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-1189-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1189-2016 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.
