Iowa Select Herbs LLC recalls White Peony Root products due to misbranding, unapproved status, and adulteration as dietary supplements. Affected items include various sizes sold online with specific lot numbers.
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 white peony root supplements because they are misbranded, unapproved as dietary supplements, and adulterated. This means the products are not legally compliant and could pose health risks.
The products are misbranded (labeled incorrectly), unapproved as dietary supplements (not approved by the FDA), and adulterated (containing harmful substances). This makes them unsafe for consumption and potentially harmful to health.
Anyone who purchased Iowa Select Herbs white peony root supplements online between the specified dates. People using these products for health purposes are most at risk due to the unapproved status.
Check for products labeled 'White Peony Root (Paeonia lactiflora)' from Iowa Select Herbs LLC, sold online with sizes ranging from 1 fl. Oz. to 40 fl. Oz. The lot number '111001H209' expires February 2020.
Look for the lot number '111001H209' and expiration date of February 2020 on the product label.
The products are misbranded, unapproved as dietary supplements, and adulterated, meaning they do not meet legal standards for safety and labeling.
The recall record does not specify a remedy, so contact Iowa Select Herbs LLC directly for guidance.
Yes, the affected products include sizes from 1 fl. Oz. to 40 fl. Oz. with lot number '111001H209' that expires February 2020.
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-1229-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1229-2016 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.
