Iowa Select Herbs LLC recalls dandelion root supplements due to misbranding, unapproved drug status, and adulteration. Consumers should stop using affected lots.
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 dandelion root supplements because they are misbranded, unapproved as new drugs, and adulterated dietary supplements. This recall follows a court order to address these violations.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (contaminated with unsafe substances). This violates federal food safety laws and poses health risks.
Anyone who purchased the recalled dandelion root supplements from Iowa Select Herbs' website. People using these products for health purposes are most at risk due to the unapproved drug status.
Check for the product name 'Dandelion Root', 1-gallon size, and lot numbers: 30902, 32945, 20792, or 33154 (all expire by September 2019).
Discard any recalled dandelion root supplements with the listed lot numbers.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, which violates federal food safety laws.
Check for the product name 'Dandelion Root', 1-gallon size, and lot numbers: 30902, 32945, 20792, or 33154 (all expire by September 2019).
Discard the product immediately as it is misbranded, unapproved, and adulterated.
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-1169-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1169-2016 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.
