Iowa Select Herbs LLC is recalling lemon balm leaf supplements due to misbranding, unapproved status, and adulteration. 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 lemon balm leaf supplements because they are misbranded, unapproved new drugs, and adulterated dietary supplements. This recall follows a court order to address these violations.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated dietary supplements (containing harmful substances). This violates federal food safety laws.
Anyone who purchased lemon balm leaf supplements from Iowa Select Herbs LLC between the specified dates. Consumers with the product are most at risk due to the legal violations.
Check for the brand 'Iowa Select Herbs' and product names like Lemon Balm Leaf (Melissa officinalis). Look for lot numbers and expiration dates on the label, such as lot 32700 expiring February 2020.
Look for the lot number and expiration date on the product label to confirm if it's part of the recall.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, as ordered by a court consent decree.
Check for the brand 'Iowa Select Herbs' and product names like Lemon Balm Leaf (Melissa officinalis) with lot numbers such as 32700 expiring February 2020.
The official recall notice does not specify a remedy or action steps beyond checking the product label.
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-1190-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1190-2016 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.
