Iowa Select Herbs LLC recalls Yohimbe Bark products as misbranded, unapproved new drugs and adulterated dietary supplements under a consent decree. 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 Yohimbe Bark products because they are misbranded, unapproved new drugs, and adulterated dietary supplements. 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.
Anyone who purchased Iowa Select Herbs Yohimbe Bark products labeled with lot number 32533, which expire by April 2018, is affected. People using these products for dietary supplements or medicinal purposes are at risk.
Check for products labeled 'Yohimbe Bark (Pausinystalia Yohimbe)' from Iowa Select Herbs LLC with lot number 32533 and an expiration date of April 2018. Products sold online at www.iowaselectherbs.com are included.
Look for lot number 32533 and expiration date of April 2018 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a consent decree.
Check for products labeled 'Yohimbe Bark (Pausinystalia Yohimbe)' from Iowa Select Herbs LLC with lot number 32533 and expiration date April 2018.
The recall record does not specify a remedy, so contact the manufacturer 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-1233-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1233-2016 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.
