Good Herbs Inc. recalls TRIPHALA herbs from October 17, 2013 onward due to not meeting Good Manufacturing Practices. Consumers should check product labels for affected lots.
Products not manufactured under GMP's
Good Herbs Inc. is recalling TRIPHALA herbal products made on or after October 17, 2013 because they were not manufactured under Good Manufacturing Practices. 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 standards for ensuring product safety and quality. This could lead to potential quality issues, but the recall does not specify a risk of serious injury or illness.
People who purchased TRIPHALA herbal products from Good Herbs Inc. on or after October 17, 2013 are affected. Those using these products for medicinal purposes may be at slightly higher risk due to quality concerns.
Check for the product name 'TRIPHALA', 1 oz bottle, and the lot date of October 17, 2013 or later. The products were distributed by Good Herbs Inc. from their Troy, MI address.
Look for the lot date of October 17, 2013 or later on the product label.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality.
Check the product label for the lot date. If it's October 17, 2013 or later, you should stop using it and contact Good Herbs Inc. for further instructions.
The recall does not specify a risk of serious injury or illness. The hazard is related to potential quality issues, not immediate safety risks.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0432-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0432-2015 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.
