Good Herbs Inc. recalls prostate support supplements made after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check product labels for the recall.
Products not manufactured under GMP's
Good Herbs Inc. is recalling prostate support supplements produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could pose a risk of contamination or unsafe ingredients.
Products not made under Good Manufacturing Practices (GMPs) may have unsafe ingredients or contamination. This could lead to health issues, but the risk is not severe enough to cause serious injury.
People who bought Good Herbs Prostate Support supplements from October 17, 2013, onward are affected. Those with health conditions requiring supplements may be at slightly higher risk.
Check for the product name 'Prostate Support', 1 oz bottle, and the distribution date of October 17, 2013 or later. The address on the label is 550 Oliver Dr Troy, MI 48084.
Look for the product name 'Prostate Support', 1 oz bottle, and the distribution date of October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs).
The recall record does not specify a remedy, so check the product label for the distribution date and contact Good Herbs Inc. for further instructions.
The recall states the products were not made under GMPs, but does not mention a risk of serious injury. The danger level is low risk.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0389-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0389-2015 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.