Iowa Select Herbs LLC recalls Alisma Leaf dietary supplements due to misbranding, unapproved status, and adulteration. 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 its Alisma Leaf dietary supplements because they are misbranded, unapproved as new drugs, and adulterated. This recall affects products sold online through their website and may pose risks if used without proper approval.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (containing harmful substances). This can lead to health risks if used without proper oversight.
Anyone who purchased Iowa Select Herbs Alisma Leaf supplements from their website. People using these products for health purposes without regulatory approval are at risk.
Check for the product name 'Alisma Leaf', brand 'Iowa Select Herbs', and lot number 130601H040. Products were sold online through the company's website and expired by February 2019.
Look for the lot number 130601H040 and expiration date of February 2019 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a consent decree.
Check for the product name 'Alisma Leaf', brand 'Iowa Select Herbs', and lot number 130601H040. Products were sold online through the company's website and expired by February 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-1137-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1137-2016 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.
