Iowa Select Herbs LLC recalls Geen Tea Leaf 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 their Geen Tea Leaf 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 (containing harmful substances). This violates federal food safety laws and poses potential health risks.
Anyone who purchased Iowa Select Herbs Geen Tea Leaf products from their website or retail stores. People who consume these products are at risk due to the unapproved and adulterated nature of the supplements.
Check for the product name 'Geen Tea Leaf', 7.5 fl. oz. size, and the lot number 32513 with an expiration date of February 2019. The products were sold online at www.iowaselectherbs.com and in stores in Cedar Rapids, IA.
Look for the lot number 32513 and expiration date of February 2019 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a court consent decree.
Check for the product name 'Geen Tea Leaf', 7.5 fl. oz. size, lot number 32513, and expiration date of February 2019.
The recall record does not specify a remedy, so contact Iowa Select Herbs LLC for guidance.
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-1182-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1182-2016 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.
