Good Herbs Inc. recalls ELEUTHERO herbal products made 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 ELEUTHERO herbal bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall is due to potential quality issues with the products.
Products not manufactured under Good Manufacturing Practices (GMPs) may have quality issues that could affect safety and effectiveness. This means the herbs might not meet the intended standards for purity and potency.
Anyone who owns or uses Good Herbs ELEUTHERO herbal products made on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to quality concerns.
Check for the product name 'ELEUTHERO', 1 or 4 oz bottles, and the production date of October 17, 2013 or later. The products were distributed by Good Herbs Inc. from their Troy, MI address.
Look for the production date on the label, which should be October 17, 2013 or later for affected products.
Reach out to Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084 for more information or to report concerns.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could affect their safety and effectiveness.
Check the production date on the label. If it's October 17, 2013 or later, contact Good Herbs Inc. for further instructions.
The recall is due to potential quality issues, not a direct 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-0183-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0183-2015 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.
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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.