Iowa Select Herbs LLC recalls 1-gallon Juniper Berry products due to misbranding, unapproved drug status, and adulteration. Consumers should avoid these products as they are unsafe dietary supplements.
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 LLC is recalling all 1-gallon Juniper Berry products because they are misbranded, unapproved as new drugs, and adulterated dietary supplements. This makes them unsafe for consumption.
The products are misbranded, meaning they don't match their labeling. They are also unapproved new drugs and adulterated dietary supplements, which means they are unsafe for consumption and could cause health issues.
Anyone who purchased the 1-gallon Juniper Berry products from Iowa Select Herbs LLC online or in stores. People using these products for dietary supplements are most at risk.
Check for the 1-gallon Juniper Berry product from Iowa Select Herbs LLC, which has a lot number of 19836 and expires May 2019. The products were sold online and in stores in Cedar Rapids, Iowa.
Look for the lot number 19836 and expiration date of May 2019 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, which makes them unsafe for consumption.
The recall record does not specify a remedy, so there is no action required beyond avoiding the product.
These products were sold online and in stores in Cedar Rapids, Iowa.
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-1188-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1188-2016 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.
