Iowa Select Herbs LLC is recalling 4 fl oz beet root products due to misbranding, unapproved drug status, and adulteration. Consumers should stop using these products immediately.
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 their beet root dietary supplements because they are misbranded, unapproved as new drugs, and adulterated. This means the products are unsafe and should not be used.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (contaminated with unsafe substances). This makes them unsafe for consumption.
Anyone who purchased Iowa Select Herbs beet root supplements from their website or stores. People using these products for dietary supplements are most at risk.
Check for the brand 'Iowa Select Herbs', product name 'Beet Root (Beta vulgaris)', size '4 fl. Oz.', and lot number '22351' with an expiration date of August 2019.
Immediately stop using all recalled Iowa Select Herbs beet root supplements.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a consent decree.
Check for the brand 'Iowa Select Herbs', product name 'Beet Root (Beta vulgaris)', size '4 fl. Oz.', lot number '22351', and expiration date of August 2019.
Stop using it immediately and contact Iowa Select Herbs for further instructions.
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-1145-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1145-2016 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.
