Iowa Select Herbs LLC recalls Momordica 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 Momordica Leaf dietary supplements because they are misbranded, unapproved as new drugs, and adulterated. This recall is required by a court order to address safety and regulatory violations.
The products are misbranded (labeled incorrectly), unapproved as new dietary supplements, and adulterated (containing harmful substances not declared). This violates federal food safety laws and poses potential health risks.
Anyone who purchased Iowa Select Herbs Momordica Leaf supplements from their website or retail stores. People using these products for health purposes are most at risk due to the unapproved and adulterated nature.
Check for the product name 'Momordica Leaf', brand 'Iowa Select Herbs', and lot number 58545F. The products were sold online at www.iowaselectherbs.com and expire by June 2019.
Look for the lot number 58545F and expiration date of June 2019 on the product label.
The products are misbranded, unapproved as new dietary supplements, and adulterated, which violates federal regulations and requires a court-ordered recall.
Check for the product name 'Momordica Leaf', brand 'Iowa Select Herbs', and lot number 58545F with an expiration date of June 2019.
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-1197-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1197-2016 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.
