Iowa Select Herbs LLC recalls Suma Root dietary supplements due to misbranding, unapproved status, and adulteration. Consumers should check product labels for lot number 21035 expiring 02/2019.
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 LLC is recalling Suma Root dietary supplements because they are misbranded, unapproved as new drugs, and adulterated. This means the product does not meet safety or labeling standards and could pose health risks.
The product is misbranded (incorrect labeling), unapproved as a new drug (not approved by the FDA), and adulterated (containing unsafe substances). This combination violates food safety and labeling laws, potentially causing health issues.
Anyone who purchased Suma Root from Iowa Select Herbs LLC online or in-store. People using dietary supplements for health purposes are most at risk due to potential health impacts from unapproved ingredients.
Check for the product name 'Suma Root', 1-gallon size, and lot number 21035 that expires February 2019. The product was sold online through www.iowaselectherbs.com and in stores in Cedar Rapids, IA.
Look for lot number 21035 and expiration date of February 2019 on the product label.
The product is misbranded, unapproved as a new drug, and adulterated, which violates food safety and labeling laws.
Check for the product name 'Suma Root', 1-gallon size, lot number 21035, and expiration date of February 2019.
The recall record does not specify a remedy, so contact Iowa Select Herbs LLC 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-1226-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1226-2016 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.
