Good Herbs Inc. recalls gentian flower essence bottles made after October 17, 2013 due to lack of 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 gentian flower essence bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall does not pose a direct health risk but ensures product quality standards.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This means the bottles might not meet the required quality levels for herbal products, but there is no indication of immediate health risks.
Anyone who owns or uses Good Herbs Inc. gentian flower essence bottles made on or after October 17, 2013. People using these products for herbal remedies may be at risk if the bottles were not manufactured under proper quality standards.
Check for the product name 'Flower Essence Gentian', 1 or 4 oz bottles, and the distribution date of October 17, 2013 or later. The bottles were distributed from 550 Oliver Dr, Troy, MI 48084.
Look for the distribution date on the bottle label, which should be October 17, 2013 or later.
Reach out to Good Herbs Inc. for further assistance or to confirm if your product is affected.
The recall indicates the products were not made under Good Manufacturing Practices, but there is no mention of health risks. The company states these products are safe for use as long as they meet quality standards.
Check the distribution date on the bottle label. If it's October 17, 2013 or later, contact Good Herbs Inc. for further instructions.
The recall does not mention any health risks, only that the products were not manufactured under Good Manufacturing Practices.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0217-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0217-2015 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.