Iowa Select Herbs LLC recalls bilberry leaf supplements due to misbranding, unapproved status, and adulteration. Consumers should check product labels for lot number 19889 expiring May 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 bilberry leaf supplements because they are misbranded, unapproved as dietary supplements, 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 as dietary supplements (not approved by the FDA), and adulterated (containing harmful substances). This means they don't meet safety or labeling standards and could cause health issues.
Anyone who purchased Iowa Select Herbs bilberry leaf supplements (4 fl. oz. or 1 gallon) with lot number 19889, expiring May 2019. People using these products for health purposes are most at risk.
Check for the product name 'Bilberry Leaf (Vaccinium myrtulli)', size (4 fl. oz. or 1 gallon), and lot number 19889 expiring May 2019 on the label.
Look for the lot number 19889 and expiration date of May 2019 on the product label.
The products are misbranded, unapproved as dietary supplements, and adulterated, meaning they do not meet safety or labeling requirements.
Check the product label for lot number 19889 expiring May 2019. If you have it, contact Iowa Select Herbs LLC for guidance.
The recall record does not specify a remedy, so consumers should check the product label and contact the manufacturer for further instructions.
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-1146-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1146-2016 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.
