Iowa Select Herbs LLC recalls Damiana Leaf supplements as misbranded, unapproved new drugs and adulterated dietary supplements under a consent decree. Consumers should check product details and contact the company for guidance.
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 Damiana Leaf (Turnera diffusa) dietary supplements because they are misbranded, unapproved new drugs, and adulterated. This recall follows a court order requiring the company to remove these products from the market.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (containing harmful substances). This violates federal regulations and poses potential health risks to consumers.
Anyone who purchased Iowa Select Herbs Damiana Leaf supplements from the company's website or retail locations in Cedar Rapids, IA. People using these supplements for health purposes may be at risk due to the unapproved and adulterated nature of the product.
Check for the product name 'Damiana Leaf (Turnera diffusa)', the website www.iowaselectherbs.com, and the lot number 31265 with an expiration date of April 2017. The product was sold in Cedar Rapids, IA.
Look for the lot number 31265 and expiration date of April 2017 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a consent decree.
Check for the lot number 31265 and expiration date of April 2017 on the product label.
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-1167-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1167-2016 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.
