Good Herbs Inc. recalls STONEROOT 1 oz bottles made on or after Oct 17, 2013 due to not being manufactured under GMPs. Consumers should check product details and contact the company.
Products not manufactured under GMP's
Good Herbs Inc. is recalling STONEROOT herbal products made on or after October 17, 2013 because they were not produced under Good Manufacturing Practices (GMPs). This means the products may not meet safety standards for food products.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety. This could mean the products do not meet the required safety standards for food products, but does not indicate an immediate risk of injury or illness.
Anyone who purchased Good Herbs STONEROOT herbal products made on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to potential safety concerns.
Check for the product name 'STONEROOT', 1 oz bottle, and the manufacturing date of October 17, 2013 or later. The products were distributed by Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084.
Look for the product name 'STONEROOT', 1 oz bottle, and the manufacturing date of October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety.
Check for the product name 'STONEROOT', 1 oz bottle, and the manufacturing date of October 17, 2013 or later.
The recall record 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-0426-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0426-2015 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.
