Good Herbs Inc. recalls Yellow Dock herb bottles made on or after Oct 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their bottles for the date and serial number.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Yellow Dock herb bottles made on or after October 17, 2013 because they were not produced under Good Manufacturing Practices. This could mean the product isn't safe for consumption.
Products not manufactured under Good Manufacturing Practices (GMPs) may not meet safety standards. This could lead to contamination or improper labeling that affects product quality and safety.
Anyone who purchased Good Herbs Yellow Dock herb bottles made on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk.
Check for the bottle label with 'Good Herbs, Inc.' and the product name 'YELLOW DOCK'. Look for the distribution date on the bottle, which is October 17, 2013 or later.
Look for the distribution date on the bottle, which is October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could affect safety and quality.
The recall record does not specify a remedy, so no action is required beyond checking the product date.
Check for the bottle label with 'Good Herbs, Inc.' and the product name 'YELLOW DOCK', and look for the distribution date on the bottle (October 17, 2013 or later).
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0450-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0450-2015 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.