Iowa Select Herbs LLC recalls alfalfa leaf supplements due to misbranding and being unapproved 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 alfalfa leaf supplements because they are misbranded and unapproved as dietary supplements. This means the products may not meet safety or labeling requirements, posing potential risks to consumers.
The products are misbranded and unapproved as dietary supplements, meaning they do not meet federal safety or labeling standards. This could lead to health risks if the supplements contain unsafe ingredients or are not properly labeled.
Anyone who purchased Iowa Select Herbs alfalfa leaf supplements (7.5 fl. oz.) from their website or stores. People using these supplements for dietary purposes are most at risk.
Check for the product name 'Alfalfa Leaf (Medicago sativa)', 7.5 fl. oz. size, and the lot number 30464 with an expiration date of February 2019. The products were sold online through Iowa Select Herbs' website.
Look for the product name, size, lot number, and expiration date on the packaging.
The products are misbranded and unapproved as dietary supplements, meaning they do not meet federal safety or labeling standards.
Check the product details and contact Iowa Select Herbs for guidance on next steps.
The recall notice does not specify a deadline for action.
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-1136-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1136-2016 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.