Iowa Select Herbs LLC recalls Lobelia Leaf products as misbranded, unapproved new drugs and adulterated dietary supplements. Consumers should check product details and contact the company for more information.
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 Lobelia Leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements. This recall is required by a consent decree to address legal violations.
The products are misbranded, meaning they do not meet labeling requirements. They are also unapproved new drugs and adulterated dietary supplements, which means they were not approved by the FDA and contain harmful substances.
Anyone who purchased Iowa Select Herbs Lobelia Leaf products from the company's website or stores. People using these products for dietary supplements or herbal remedies are most at risk.
Check for the product name 'Lobelia Leaf', brand 'Iowa Select Herbs', and lot number 31266. Products were sold online at www.iowaselectherbs.com and expire by June 2019.
Look for the lot number 31266 and expiration date of June 2019 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as required by a consent decree for injunctive relief.
Check for the product name 'Lobelia Leaf', brand 'Iowa Select Herbs', and lot number 31266. Products were sold online at www.iowaselectherbs.com and expire by June 2019.
The recall record does not specify a remedy, so contact Iowa Select Herbs LLC for further instructions.
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-1192-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1192-2016 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.
