Iowa Select Herbs LLC recalls Quack Grass dietary supplement due to misbranding and being an unapproved new drug. Consumers should check product labels for lot number 20668 expiring 12/2019.
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 its Quack Grass dietary supplement because it's misbranded and unapproved as a new drug. This means the product isn't legally approved for sale and could be unsafe.
The product is misbranded and unapproved as a dietary supplement, meaning it doesn't meet legal standards for safety and labeling. It's also classified as an adulterated dietary supplement, which can pose health risks if not properly regulated.
Anyone who purchased Iowa Select Herbs Quack Grass from www.iowaselectherbs.com. People using dietary supplements for health purposes may be at risk due to the unapproved status.
Check for the product name 'Quack Grass' on the label. Look for the lot number 20668 with an expiration date of December 2019. The product was sold online through www.iowaselectherbs.com.
Look for the lot number 20668 and expiration date of December 2019 on the product label.
The product is misbranded and unapproved as a dietary supplement, so it may not be safe. The recall is due to legal issues with labeling and approval.
Check for the lot number 20668 with an expiration date of December 2019 on the label. The product was sold online through www.iowaselectherbs.com.
The recall record does not specify a remedy, so there is no action required beyond checking if you have the product.
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-1213-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1213-2016 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.
