Iowa Select Herbs LLC recalls Rhodiola Root products due to misbranding, unapproved status, and adulteration as dietary supplements. 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 Rhodiola Root products because they are misbranded, unapproved as dietary supplements, and adulterated. This means the products do not meet safety or labeling standards and could pose health risks.
The products are misbranded (incorrect labeling), unapproved as dietary supplements (not approved by the FDA), and adulterated (containing unsafe ingredients). This can lead to health risks if used without proper oversight.
Anyone who purchased Rhodiola Root from Iowa Select Herbs LLC online or in stores. People using these products for health purposes may be at risk due to the unapproved status.
Check for the brand 'Iowa Select Herbs' and product name 'Rhodiola Root' on the label. The product was sold online at www.iowaselectherbs.com and in stores with a lot number starting with 131101H504 and expiration date 12/2019.
Look for the lot number starting with 131101H504 and expiration date 12/2019 on the product label.
The products are misbranded, unapproved as dietary supplements, and adulterated, which means they do not meet safety or labeling standards.
Check for the brand 'Iowa Select Herbs' and product name 'Rhodiola Root' with lot number starting with 131101H504 and expiration date 12/2019.
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-1216-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1216-2016 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.
