Iowa Select Herbs LLC recalls bitter melon products due to misbranding, unapproved drug 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 LLC is recalling bitter melon products because they are misbranded, unapproved as new drugs, and adulterated dietary supplements. This recall follows a court order to address these issues.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (containing harmful substances). This violates federal regulations and poses potential health risks.
Anyone who purchased Iowa Select Herbs bitter melon products from the company's website or stores. Consumers most at risk are those who have used the products without knowing they were unapproved supplements.
Check for the product name 'Bitter Melon (Momordica charantia)', 32 fl. oz. size, and the lot number -58545F. The products were sold online at www.iowaselectherbs.com and expired by May 2019.
Look for the lot number -58545F and expiration date of May 2019 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as ordered by a court consent decree.
Check for the product name 'Bitter Melon (Momordica charantia)', 32 fl. oz. size, and lot number -58545F on the label.
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-1147-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1147-2016 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.
