Iowa Select Herbs LLC recalls Black Cohosh Root products as misbranded, unapproved new drugs and adulterated dietary supplements under a consent decree. 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 is recalling Black Cohosh Root products because they are misbranded, unapproved new drugs, and adulterated dietary supplements. This recall follows a court-ordered consent decree to address unsafe product practices.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (containing harmful substances). This violates federal regulations and poses potential health risks.
Anyone who purchased Iowa Select Herbs Black Cohosh Root products from their website or stores. People using these products for dietary supplements are most at risk due to the unapproved and misbranded nature.
Check for the product name 'Black Cohosh Root', 1 fl. Oz. size, and the lot number 19972 with an expiration date of August 2019 on the packaging. The products were sold online at www.iowaselectherbs.com.
Look for the lot number 19972 and expiration date of August 2019 on the packaging.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a court consent decree.
Check for the product name 'Black Cohosh Root', 1 fl. Oz. size, lot number 19972, and expiration date of August 2019 on the packaging.
The recall record does not specify a remedy, so contact Iowa Select Herbs LLC directly 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-1148-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1148-2016 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.
