Good Herbs Inc. recalls SPLEEN SUPPORT herbal supplements from October 2013 with unverified manufacturing standards. Consumers should check product dates and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling SPLEEN SUPPORT herbal supplements produced on or after October 17, 2013, because they were not made under Good Manufacturing Practices. This could mean the product might not be safe or effective.
The product was not manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety and quality. This could mean the supplement might not be safe or effective as intended, but it does not indicate an immediate risk of injury or illness.
People who bought Good Herbs SPLEEN SUPPORT herbal supplements from October 17, 2013, onward are affected. Those using the product for health reasons may be at slightly higher risk due to unverified quality.
Check for the product name 'SPLEEN 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 distribution date on the label, which should be October 17, 2013 or later.
Reach out to Good Herbs Inc. for further details about the recall and any necessary actions.
The recall states the product was not manufactured under Good Manufacturing Practices, which could mean it might not be safe or effective, but it does not indicate an immediate risk of injury.
Check for the product name 'SPLEEN 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.
Contact Good Herbs Inc. for details on the recall and any necessary actions.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0420-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0420-2015 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.
