Iowa Select Herbs LLC recalls marshmallow root supplements due to misbranding, unapproved status, and adulteration. Consumers should check product labels for 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 marshmallow root supplements that are misbranded, unapproved as dietary supplements, and adulterated. This means the products do not meet safety or labeling requirements 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 means they do not meet safety or labeling standards and could cause health issues.
Anyone who purchased Iowa Select Herbs marshmallow root supplements (4 fl. oz. or 16 fl. oz.) between the time of sale and expiration date (April 2019). People using these products for health purposes are most at risk.
Check for the brand 'Iowa Select Herbs' and product names 'Marshmallow Root (Althaea officinalis)'. Look for lot number 30933 and expiration date April 2019 on the label.
Look for the lot number 30933 and expiration date of April 2019 on the product label.
The products are misbranded, unapproved as dietary supplements, and adulterated, meaning they do not meet safety or labeling requirements.
Check the product label for lot number 30933 and expiration date April 2019. If it matches, contact Iowa Select Herbs for guidance.
The recall is due to misbranding and unapproved status, not a direct risk of serious injury. The danger level is low risk.
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-1194-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1194-2016 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.
