Iowa Select Herbs LLC recalls Reishi Mushroom (Ganoderma Lucidum) products as misbranded, unapproved new drugs and adulterated dietary supplements. Consumers should check product details and contact the company for guidance.
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 their Reishi Mushroom (Ganoderma Lucidum) dietary supplements because they are misbranded, unapproved new drugs, and adulterated. This recall is required by a consent decree to address legal violations in product labeling and safety.
The products are misbranded (incorrect labeling), unapproved new drugs (not approved by the FDA), and adulterated (containing harmful substances). This violates federal food safety laws and could pose health risks.
Anyone who purchased Iowa Select Herbs Reishi Mushroom (Ganoderma Lucidum) products from the company's website or stores. Consumers who have the product are most at risk due to the legal violations.
Check for the product name 'Reishi Mushroom (Ganoderma Lucidum)', 7.5 fl. oz. size, and the lot number 8427 with an expiration date of February 2020. The products were sold online at www.iowaselectherbs.com.
Look for the product name, size, lot number, and expiration date on the packaging.
The products are misbranded, unapproved new drugs, and adulterated, which violates federal food safety laws and requires a recall under a consent decree.
Check for the product name 'Reishi Mushroom (Ganoderma Lucidum)', 7.5 fl. oz. size, lot number 8427, and expiration date of February 2020.
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-1215-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1215-2016 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.
