Iowa Select Herbs LLC recalls Sassparilla Smilax uti lis products as misbranded, unapproved dietary supplements. Consumers should check product labels for lot number 30709 expiring July 2019.
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 Sassparilla Smilax uti lis products because they are misbranded and unapproved as dietary supplements. This means the products are not legally approved for sale and could be unsafe.
The products are misbranded and unapproved as dietary supplements, meaning they were not legally approved by the FDA for sale. This could lead to unsafe ingredients or improper labeling that might cause health issues.
Anyone who purchased Iowa Select Herbs Sassparilla Smilax uti lis products with lot number 30709 expiring July 2019. People using these products for health purposes may be at risk due to unapproved ingredients.
Check product labels for the lot number 30709 and expiration date of July 2019. The product is sold online at www.iowaselectherbs.com and comes in 7.5 fl. oz. size.
Look for lot number 30709 and expiration date of July 2019 on the product label.
The products are misbranded and unapproved as dietary supplements, meaning they were not legally approved by the FDA for sale.
The official recall notice does not specify a remedy, so check the product label for lot number 30709 expiring July 2019 and contact Iowa Select Herbs LLC for further instructions.
The products are unapproved dietary supplements, which could pose health risks due to unsafe ingredients or improper labeling.
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-1220-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1220-2016 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.
