Iowa Select Herbs LLC recalls 7.5 fl. oz. turmeric products due to misbranding, unapproved drug status, and adulteration. Consumers should check lot numbers and expiration dates.
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 turmeric products because they are misbranded, unapproved as dietary supplements, and adulterated. This means the products may not be safe or legally compliant.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (containing unsafe ingredients). This makes them legally non-compliant but does not necessarily cause immediate health risks.
Anyone who purchased Iowa Select Herbs turmeric products between the product's sale date and expiration (July 2020). The risk is low as the hazard relates to legal compliance rather than direct health harm.
Check for the brand 'Iowa Select Herbs', product name 'Tumeric', 7.5 fl. oz. size, and lot number 37441 with an expiration date of July 2020.
Look for the lot number 37441 and expiration date of July 2020 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as ordered by a consent decree for injunctive relief.
Check the product label for lot number 37441 and expiration date of July 2020. If it matches, you may not need to take action since the recall is for legal compliance, not immediate health risks.
The recall is for legal compliance reasons, not direct health risks. The products are not safe for use as dietary supplements due to being unapproved and adulterated.
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-1227-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1227-2016 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.
