Good Herbs Inc. recalls BUCKTHORN herbal products made after October 17, 2013 due to not meeting 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 BUCKTHORN herbal products sold after October 17, 2013 because they were not manufactured under Good Manufacturing Practices. This recall does not pose a direct health risk but ensures product quality standards.
The products were not made under Good Manufacturing Practices (GMPs), which are standards for food safety and quality. This means the herbs might not be as pure or potent as advertised, but there is no immediate health risk.
Anyone who purchased Good Herbs BUCKTHORN herbal products from stores or online after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for the product name 'BUCKTHORN' and the size (1 or 4 oz bottle). The recall applies to all lots distributed on or after October 17, 2013.
Look for the distribution date on the product label; recall applies to items made on or after October 17, 2013.
Reach out to Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084 for further assistance or to return the product.
No, the recall is due to not meeting Good Manufacturing Practices, which means the product may not be as pure or potent as advertised, but there is no immediate health risk.
Check the product label for 'BUCKTHORN' and the size (1 or 4 oz bottle). The recall applies to all lots distributed on or after October 17, 2013.
Contact Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084 to return the product or get 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-0139-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0139-2015 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
