Iowa Select Herbs LLC recalls licorice root 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 licorice root supplements because they are misbranded, unapproved as dietary supplements, and adulterated. This means the products may not be safe or legally compliant.
The products are misbranded (labeled incorrectly), unapproved as dietary supplements (not approved by the FDA), and adulterated (containing harmful substances). This makes them potentially unsafe for consumption.
Anyone who purchased Iowa Select Herbs licorice root supplements (2 fl. oz., 4 fl. oz., or 16 fl. oz.) with lot numbers 32698 or 33380 expiring February 2020. People using these products for health purposes are most at risk.
Check for lot numbers 32698 or 33380 on the label, which expire February 2020. Products sold online at www.iowaselectherbs.com are affected.
Look for lot numbers 32698 or 33380 that expire February 2020 on the label.
The products are misbranded, unapproved as dietary supplements, and adulterated, which makes them potentially unsafe.
Check the product label for lot numbers 32698 or 33380 expiring February 2020. If you have these, contact Iowa Select Herbs for guidance.
The recall record does not specify a remedy, so consumers should check with the manufacturer for further instructions.
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-1191-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1191-2016 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.
