Good Herbs Inc. recalls Para Formula 2 herbal supplements made after October 17, 2013 due to failure to meet Good Manufacturing Practices. Consumers should check their bottles for the lot date.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Para Formula 2 herbal supplements produced on or after October 17, 2013 because they were not made 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 mean the supplements might not be as effective or could contain harmful substances.
Anyone who owns or uses Para Formula 2 herbal supplements purchased on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for the product name 'Para Formula 2', 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 on the bottle, which should be October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality.
Check the lot date on the bottle; if it's October 17, 2013 or later, contact Good Herbs Inc. for further instructions.
The recall is due to potential quality issues, but there is no specific mention of serious injury risk in the official notice.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0373-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0373-2015 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.
