Iowa Select Herbs LLC recalls Alcohol-Free Dandelion Root products as misbranded, unapproved new drugs and adulterated dietary supplements under a consent decree.
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 its Alcohol-Free Dandelion Root products because they are misbranded, unapproved new drugs, and adulterated dietary supplements. This recall follows a court-ordered consent decree to address these 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 regulations and poses potential health risks.
Anyone who purchased Iowa Select Herbs Alcohol-Free Dandelion Root products from their website or stores in Cedar Rapids, IA. People using these products for dietary supplements are most at risk.
Check for the product name 'Alcohol-Free Dandelion Root', 1-gallon size, and the lot number 20792 with an expiration date of April 2020 on the label.
Look for the lot number 20792 and expiration date of April 2020 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as ordered by a consent decree.
The recall record does not specify a remedy, so check the product label for the lot number and expiration date to confirm if it's affected.
The recall record does not specify a deadline for action.
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-1235-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1235-2016 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.
