Iowa Select Herbs LLC recalls 4 fl oz Acerola Berry supplements due to misbranding, unapproved status, and adulteration. Consumers should check product details and contact the company for guidance.
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 their Acerola Berry dietary supplements because they are misbranded, unapproved as new drugs, and adulterated. This means the products may not be safe or legally compliant, and consumers should stop using them.
The products are misbranded (labeled incorrectly), unapproved new drugs (not approved by the FDA), and adulterated (containing unsafe substances). This makes them potentially unsafe for consumption and not legally compliant with food safety standards.
Anyone who purchased Iowa Select Herbs' 4 fl oz Acerola Berry supplements from their website or stores. People using these supplements for health purposes are most at risk due to potential safety issues.
Check for the product name 'Acerola Berry (Malpighia)', 4 fl oz (120 ml) size, and the lot number 32795 with an expiration date of April 2019. The products were sold online through Iowa Select Herbs' website.
Look for the lot number 32795 and expiration date of April 2019 on the product label.
The products are misbranded, unapproved new drugs, and adulterated, which means they are not legally compliant and could be unsafe.
Check for the product name 'Acerola Berry (Malpighia)', 4 fl oz (120 ml) size, lot number 32795, and expiration date of April 2019.
The recall record does not specify a remedy, so contact Iowa Select Herbs directly for guidance.
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-1134-2016 — Iowa Select Herbs Iowa Select Herbs Hello, I own a Iowa Select Herbs that is covered by recall F-1134-2016 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.
