Iowa Select Herbs LLC recalls Propolis Resin (Ligustrum lucidum) due to misbranding, unapproved drug status, and adulteration. 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 Propolis Resin (Ligustrum lucidum) dietary supplement because it is misbranded, unapproved as a new drug, and adulterated. This means the product does not meet safety or labeling standards and could pose health risks.
The product is misbranded (incorrect labeling), unapproved as a new drug, and adulterated (contaminated with unsafe substances). This means it may not be safe for consumption and could cause health problems.
Anyone who purchased Iowa Select Herbs Propolis Resin (Ligustrum lucidum) from their website or retail stores. People using this product for health purposes are most at risk due to potential safety issues.
Check for the product name 'Propolis Resin (Ligustrum lucidum)', 2 fl. oz. size, and the lot number 22386 with expiration date 08/2018 on the label. The product was sold online at www.iowaselectherbs.com.
Look for the lot number 22386 and expiration date 08/2018 on the product label.
The product is misbranded, unapproved as a new drug, and adulterated, meaning it does not meet safety or labeling standards.
Check for the product name 'Propolis Resin (Ligustrum lucidum)', 2 fl. oz. size, and lot number 22386 with expiration date 08/2018 on the label.
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-1210-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1210-2016 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
