Good Herbs Inc. recalls European Elder herbs sold from 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 European Elder herbal products sold from October 17, 2013, because they were not made under Good Manufacturing Practices. This recall does not pose a direct health risk but ensures product quality standards.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety and quality. This means the herbs might not meet expected quality levels, but the recall does not indicate a direct health hazard.
Anyone who purchased Good Herbs European Elder herbal products from October 17, 2013, onward. People using these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for the product name 'European Elder' and the bottle size (1 or 4 oz). The recall applies to all lots distributed on or after October 17, 2013, from Good Herbs Inc. in Troy, MI.
Look for the distribution date on the product label; recall applies to items from October 17, 2013, onward.
Reach out to Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084 for further assistance or to return the product.
The recall does not indicate a direct health hazard, but the products were not made under Good Manufacturing Practices, which may affect quality.
Check the product label for 'European Elder' and the distribution date; recall applies to items from October 17, 2013, onward.
No immediate action is required, but you should check the product date and contact Good Herbs Inc. if you have concerns.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0192-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0192-2015 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.
