Iowa Select Herbs LLC recalls Ginkgo Biloba supplements due to misbranding and being unapproved dietary supplements. Consumers should check product details and contact the company for more information.
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 Ginkgo Biloba supplements because they are misbranded and unapproved as dietary supplements. This means the products do not meet legal standards and could pose health risks.
The products are misbranded and unapproved as dietary supplements, meaning they do not meet legal standards for safety and labeling. This can lead to health risks if the supplements are used without proper oversight.
Anyone who purchased Iowa Select Herbs Ginkgo Biloba supplements from their website or retail stores. People using these supplements for health purposes are most at risk.
Check for the product name 'Ginkgo Leave (Ginkgo biloba)', 7.5 fl. oz. size, and the lot number 30520 with an expiration date of August 2018. The products were sold online through Iowa Select Herbs' website.
Look for the product name 'Ginkgo Leave (Ginkgo biloba)', 7.5 fl. oz. size, and lot number 30520 with an expiration date of August 2018.
The products are misbranded and unapproved as dietary supplements, meaning they do not meet legal standards for safety and labeling.
Check for the product name 'Ginkgo Leave (Ginkgo biloba)', 7.5 fl. oz. size, and lot number 30520 with an expiration date of August 2018.
The official recall notice does not specify a remedy or action for consumers.
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-1178-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1178-2016 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.
