Iowa Select Herbs LLC recalls Buchu Leaf products due to misbranding, unapproved drug status, and adulteration as 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 is recalling their Buchu Leaf products because they are misbranded, unapproved as new drugs, and adulterated dietary supplements. This recall is required by a court order to address illegal product claims.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated dietary supplements (containing harmful substances). This violates federal laws and poses health risks.
Anyone who purchased Iowa Select Herbs Buchu Leaf products from their website or stores. People using these products for health purposes are most at risk due to the unapproved drug status.
Check for the product name 'Buchu Leaf', brand 'Iowa Select Herbs', and lot number 30338 with an expiration date of July 2017. Products were sold online at www.iowaselectherbs.com.
Look for the lot number 30338 and expiration date of July 2017 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as ordered by a court consent decree.
Check for the lot number 30338 and expiration date of July 2017 on the product label. Products were sold online at www.iowaselectherbs.com.
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-1153-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1153-2016 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.
