Good Herbs Inc. recalls apricot herb bottles made on or 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 apricot herb bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall does not pose an immediate safety risk but is important for quality assurance.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product quality and safety. This means the herbs may not meet the expected quality levels, but there is no indication of immediate health risks.
Owners of Good Herbs apricot herb bottles with a production date of October 17, 2013 or later are affected. People using these products for herbal remedies may be at risk of receiving substandard products.
Check for the product name 'Good Herbs, Inc., APRICOT' on the bottle. The recall applies to bottles produced on or after October 17, 2013.
Look for the production date on the bottle label, which should be October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product quality and safety.
Check the production date on the bottle. If it's October 17, 2013 or later, contact Good Herbs Inc. for further instructions.
No, the recall is for quality assurance purposes, not due to a safety hazard.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0106-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0106-2015 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.
