Good Herbs Inc. recalls skullcap herbal supplements produced on or after October 17, 2013 due to failure to meet Good Manufacturing Practices. Consumers should contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling skullcap herbal supplements sold in 4-ounce bottles from October 17, 2013 onward because they were not made under proper food safety standards. This recall is due to potential quality issues that could affect product safety.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are food safety standards. This means the supplements might not meet quality and safety requirements, potentially leading to health issues if consumed.
Anyone who purchased Good Herbs skullcap herbal supplements in 4-ounce bottles from October 17, 2013 onward. People using these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for 4-ounce skullcap bottles labeled 'Good Herbs, Inc.' with a distribution date of October 17, 2013 or later. The product was sold through the company's address in Troy, Michigan.
Reach out to Good Herbs, Inc. for specific instructions on how to handle the recalled product.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are food safety standards.
Contact Good Herbs, Inc. for specific instructions on how to handle the recalled product.
The recall applies to products distributed on or after October 17, 2013.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0415-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0415-2015 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.
