Iowa Select Herbs LLC recalls 1-gallon Yucca Root (Yucca aloifolia) due to misbranding and unapproved status as a dietary supplement. Products sold online at www.iowaselectherbs.com are affected.
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 1-gallon Yucca Root products because they are misbranded and unapproved as dietary supplements. This means the products do not meet federal safety and labeling requirements.
The products are misbranded (labeled incorrectly) and unapproved as dietary supplements, meaning they do not meet federal safety and labeling requirements. This could lead to health risks if used without proper oversight.
Anyone who purchased the 1-gallon Yucca Root (Yucca aloifolia) from Iowa Select Herbs online. People using the product for dietary supplements are most at risk due to the unapproved status.
Check for the product name 'Yucca Root (Yucca aloifolia)', 1-gallon size, and the lot number 31990 with an expiration date of February 2019. Products were sold online at www.iowaselectherbs.com.
Look for the lot number 31990 and expiration date of February 2019 on the product label.
The products are misbranded and unapproved as dietary supplements, meaning they do not meet federal safety and labeling requirements.
Check for the product name 'Yucca Root (Yucca aloifolia)', 1-gallon size, and the lot number 31990 with an expiration date of February 2019.
The recall does not specify a remedy, so contact Iowa Select Herbs LLC 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-1237-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1237-2016 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.
