Good Herbs Inc. recalls intestinal health supplements from October 17, 2013, due to failure to meet Good Manufacturing Practices. Consumers should check product dates and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling intestinal health supplements sold from October 17, 2013, because they were not made under proper Good Manufacturing Practices. This could lead to unsafe products that don't meet quality standards.
The products were not made under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This means the supplements might not be as safe or effective as they should be, but the hazard does not involve immediate risks like injury or illness.
People who purchased Good Herbs Intestinal Health supplements (1 & 4 oz bottles) from October 17, 2013, onward are affected. Those using these products for health reasons may be at risk if the supplements were not manufactured to quality standards.
Check for the product name 'Intestinal Health' and the bottle size (1 or 4 oz). Products were distributed starting October 17, 2013, from the manufacturer's location in Troy, MI.
Look for the distribution date on the product label, which is October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices, which are standards for ensuring product safety and quality.
Check for the product name 'Intestinal Health' and the bottle size (1 or 4 oz). Products were distributed starting October 17, 2013.
The recall does not specify a remedy, so contact Good Herbs Inc. for further instructions.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0309-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0309-2015 from Good 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.