Iowa Select Herbs LLC recalls 1-gallon broad beans due to misbranding, unapproved drug status, and adulteration as dietary supplements. Consumers should check lot numbers and contact the company for details.
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 1-gallon broad beans 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 product is legally misbranded and unapproved as a dietary supplement, meaning it does not meet federal safety standards. It is also classified as an adulterated dietary supplement, which can pose health risks if consumed without proper regulation.
Anyone who purchased Iowa Select Herbs broad beans from their website between the product's sale date and expiration (November 2018). The risk is highest for consumers who may have used the beans as dietary supplements.
Check for the lot number 15882 on the product label. The product was sold online through Iowa Select Herbs LLC's website and expires November 2018.
Look for the lot number 15882 on the product label to confirm if it is recalled.
The product is misbranded, unapproved as a new drug, and adulterated as a dietary supplement, requiring a court-ordered recall.
Check for the lot number 15882 on the product label; the product was sold online through Iowa Select Herbs LLC's website and expires November 2018.
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-1152-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1152-2016 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.
