Iowa Select Herbs LLC recalls its Alcohol-free Sage Leaf product due to misbranding, unapproved drug status, and adulteration. Consumers should check lot numbers 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 its Alcohol-free Sage Leaf product because it is misbranded, unapproved as a new drug, and adulterated. This means the product does not meet safety or labeling standards and could pose health risks.
The product is misbranded (incorrect labeling), unapproved as a new drug, and adulterated (contaminated with unsafe substances). This means it may not be safe for consumption and could cause health issues.
Anyone who purchased Iowa Select Herbs' Alcohol-free Sage Leaf product from their website or stores. People using the product for dietary supplements are most at risk due to potential health impacts.
Check for the product name 'Alcohol-free Sage Leaf', the website www.iowaselectherbs.com, and the lot number 32880 with an expiration date of April 2020.
Look for the lot number 32880 and expiration date of April 2020 on the product label.
The product is misbranded, unapproved as a new drug, and adulterated, meaning it does not meet safety or labeling standards.
Check for the product name 'Alcohol-free Sage Leaf', the website www.iowaselectherbs.com, and the lot number 32880 with an expiration date of April 2020.
The recall record does not specify a remedy, so contact Iowa Select Herbs LLC directly 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-1218-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1218-2016 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.
