Iowa Select Herbs LLC is recalling olive leaf products due to misbranding, unapproved status, and adulteration as dietary supplements. Consumers should check product labels for lot numbers and expiration dates.
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 olive leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements. This recall affects consumers who purchased these products from the company's website or stores.
The products are misbranded, meaning they don't match their labeling. They are also unapproved new drugs and adulterated dietary supplements, which means they were not approved by the FDA and contain harmful substances.
Anyone who purchased Iowa Select Herbs olive leaf products (4 fl. oz., 16 fl. oz., or 1 gallon) from the company's website or stores. People using these products as dietary supplements are most at risk.
Check for the brand name 'Iowa Select Herbs' and product type 'Olive Leaf (Olea europa)'. Look for lot number 32772 with an expiration date of May 2019.
Look for the lot number 32772 and expiration date of May 2019 on the product label.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements as ordered by a consent decree.
The official recall notice does not specify a remedy, so check product labels for lot number 32772 and expiration date of May 2019.
The recall notice does not specify a deadline for action.
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-1201-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1201-2016 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.
