Iowa Select Herbs LLC recalls milk thistle seed supplements due to misbranding, unapproved status, and adulteration. Consumers should check product labels for specific lots 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 milk thistle seed supplements because they are misbranded, unapproved as new drugs, and adulterated. This means the products do not meet safety or labeling requirements and could pose health risks.
The products are misbranded (incorrect labeling), unapproved new drugs (not approved by the FDA), and adulterated (containing harmful substances). This makes them unsafe for consumption and violates food safety regulations.
Anyone who purchased milk thistle seed supplements from Iowa Select Herbs between the specified lots and expiration dates. People using these supplements for health purposes are most at risk due to potential safety issues.
Check for the product name 'Milk Thistle Seed (Carduus marianus)' and lot numbers: 32358, 32964, or 631H42200122. Products with expiration dates of 10/2019 are affected.
Look for lot numbers 32358, 32964, or 631H42200122 with expiration dates of 10/2019.
The products are misbranded, unapproved new drugs, and adulterated dietary supplements, which violates food safety regulations.
Check the product labels for the specific lot numbers and expiration dates mentioned. If you have the affected lots, you may need to stop using them.
Yes, the products are unapproved and adulterated, which could pose health risks if consumed.
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-1196-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1196-2016 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.
