Iowa Select Herbs LLC recalls oregano leaf products as misbranded, unapproved dietary supplements. Consumers should check product labels for lot number 19976 and expiration date 05/2018.
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 oregano leaf products because they are misbranded, unapproved dietary supplements, and adulterated. This means the products do not meet safety or labeling standards and could pose health risks.
The products are misbranded (labeled incorrectly), unapproved (not approved by regulatory authorities), and adulterated (containing harmful substances). This means they do not meet safety or labeling standards and could pose health risks.
Anyone who purchased Iowa Select Herbs oregano leaf products with lot number 19976, which expired May 2018. Consumers most at risk are those who used these products as dietary supplements without proper approval.
Check for the lot number 19976 and expiration date of May 2018 on the product label. The product is sold by Iowa Select Herbs LLC at www.iowaselectherbs.com.
Look for the lot number 19976 and expiration date of May 2018 on the oregano leaf product.
The products are misbranded, unapproved dietary supplements, and adulterated, meaning they do not meet safety or labeling standards.
Check the product label for lot number 19976 and expiration date of May 2018. If you have the product, you should stop using it and contact the manufacturer.
The recall record does not specify a remedy, so consumers should check with the manufacturer 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-1202-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1202-2016 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.
