Iowa Select Herbs LLC recalls Atragalus Root (Astragalus Membranaceus) products due to being misbranded, unapproved new drugs, and adulterated dietary supplements. Consumers should check product lots and contact the company for details.
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 Atragalus Root (Astragalus Membranaceus) products because they are misbranded, unapproved new drugs, and adulterated dietary supplements. This recall affects consumers who purchased these products from the company's website.
The products are misbranded, meaning they do not accurately describe their contents. They are also unapproved new drugs and adulterated dietary supplements, which means they were not approved by the FDA and contain harmful substances.
Anyone who purchased Iowa Select Herbs Atragalus Root products from their website between the specified lots. People using these supplements for health purposes are most at risk due to the unapproved nature of the products.
Check for product lots 31685 (expires May 2019) or 30900 (expires May 2019) on Iowa Select Herbs LLC's website. The products come in 1 fl. oz., 2 fl. oz., 4 fl. oz., and 7.5 fl. oz. sizes.
Look for lot numbers 31685 or 30900 on the product packaging.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a consent decree for injunctive relief.
Check the product lot number and contact Iowa Select Herbs LLC for further instructions.
The products are unapproved new drugs and adulterated dietary supplements, which may pose health risks, but the recall does not specify exact hazards.
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-1142-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1142-2016 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.
