Iowa Select Herbs LLC recalls Alcohol-Free Cilantro Leaf products due to misbranding, unapproved status, and adulteration as 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 its Alcohol-Free Cilantro Leaf products because they are misbranded, unapproved as dietary supplements, and adulterated. This means the products do not meet safety or labeling standards and could pose health risks.
The products are misbranded (incorrect labeling), unapproved as dietary supplements (not approved by the FDA), and adulterated (containing harmful substances). This means they may not be safe for consumption and could cause health issues.
Anyone who purchased Iowa Select Herbs Alcohol-Free Cilantro Leaf products from the company's website or stores. People using these products for dietary supplements are most at risk due to the unapproved status.
Check for the brand 'Iowa Select Herbs', product name 'Alcohol-Free Cilantro Leaf', and lot number 32446 with an expiration date of April 2020. The products were sold online at www.iowaselectherbs.com.
Look for the lot number 32446 and expiration date of April 2020 on the product label.
The products are misbranded, unapproved as dietary supplements, and adulterated, meaning they do not meet safety or labeling standards.
Check the product details to see if it matches the recall criteria. Contact Iowa Select Herbs LLC for further guidance.
The recall record 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-1160-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1160-2016 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.
