Iowa Select Herbs LLC recalls dandelion 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 dandelion leaf supplements because they are misbranded and unapproved as dietary supplements. This means the products are not legally compliant and could pose health risks if used without proper oversight.
The products are misbranded and unapproved as dietary supplements, meaning they do not meet federal safety and labeling requirements. This could lead to health risks if the product is used without proper regulatory oversight.
Anyone who purchased the dandelion leaf supplement from Iowa Select Herbs online or in stores. People using the product for health purposes may be at risk due to the unapproved status.
Check for the product name 'Dandelion Leaf (Taraxacum officinale)', 1-gallon size, and the lot number 324966 with an expiration date of September 2020. The products were sold online through www.iowaselectherbs.com.
Look for the lot number 324966 and expiration date of September 2020 on the product label.
The products are misbranded and unapproved as dietary supplements, meaning they do not meet federal safety and labeling requirements.
Check the product details for the lot number and expiration date. Contact Iowa Select Herbs LLC for further guidance.
The products are unapproved dietary supplements, which could pose health risks if used without proper regulatory oversight.
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-1168-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1168-2016 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.
