Iowa Select Herbs LLC recalls Gymnema Sylvestre supplements 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 Gymnema Sylvestre supplements because they are misbranded, unapproved as new drugs, and adulterated. This means the products may not be safe or properly labeled, and they should be stopped use immediately.
The products are misbranded (incorrectly labeled), unapproved new drugs (not approved by the FDA), and adulterated (contaminated with unsafe substances). This makes them potentially unsafe for consumption and could cause health risks.
Anyone who purchased the 2 fl. oz. or 4 fl. oz. Gymnema Sylvestre supplements from Iowa Select Herbs online or in stores. People using these products for health reasons are most at risk due to potential safety issues.
Check for the brand 'Iowa Select Herbs' and product names 'Gymnema Sylvestre' with sizes 2 fl. oz. or 4 fl. oz. Look for lot number m10866 and expiration date 02/2019 on the packaging.
Immediately stop using the recalled Gymnema Sylvestre supplements as they are misbranded, unapproved, and adulterated.
These products are misbranded (incorrectly labeled), unapproved new drugs, and adulterated (contaminated with unsafe substances) as ordered by a consent decree.
Stop using them immediately and do not consume the products.
Look for the brand 'Iowa Select Herbs', product name 'Gymnema Sylvestre', sizes 2 fl. oz. or 4 fl. oz., lot number m10866, and expiration date 02/2019 on the packaging.
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-1183-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1183-2016 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.
