Iowa Select Herbs LLC recalls Alcohol-Free Cyperus Leaf dietary supplements due to misbranding and being unapproved new drugs. Consumers should check product labels for lot number 06305SL12.
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 its Alcohol-Free Cyperus Leaf dietary supplements because they are misbranded and unapproved as new drugs. This means the products are not legally approved for sale and could be unsafe.
The products are misbranded and unapproved as new dietary supplements. This means they do not meet federal safety and labeling requirements, which could lead to health risks if used without proper oversight.
Anyone who purchased Iowa Select Herbs Alcohol-Free Cyperus Leaf supplements from their website or stores. People using these products for dietary supplements are most at risk.
Check for the product name 'Alcohol-Free Cyperus Leaf', 1-gallon size, and lot number 06305SL12 on the label. The product was sold online through Iowa Select Herbs' website and expires April 2020.
Look for the lot number 06305SL12 on the label to confirm if the product is recalled.
The products are misbranded and unapproved as new dietary supplements, which means they do not meet federal safety and labeling requirements.
Check the product label for lot number 06305SL12. If it matches, contact Iowa Select Herbs for guidance.
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-1166-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1166-2016 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.
