Good Herbs Inc. recalls GYMNEMA 1 & 4 oz bottles made on or after October 17, 2013 for not meeting Good Manufacturing Practices. Consumers should check product labels for affected lots.
Products not manufactured under GMP's
Good Herbs Inc. is recalling GYMNEMA herbal bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall does not pose a direct health risk but addresses potential quality issues with the product.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This could mean the herbal supplements may not meet expected quality levels, but does not indicate a direct health hazard.
Owners of Good Herbs GYMNEMA herbal bottles with 1 or 4 oz capacity purchased on or after October 17, 2013 are affected. People using these products for herbal supplements are most at risk due to potential quality concerns.
Check for the product name 'GYMNEMA', 1 or 4 oz bottle size, and the lot date of October 17, 2013 or later. The product was distributed by Good Herbs Inc. from their Troy, MI address.
Look for the product name 'GYMNEMA', 1 or 4 oz bottle size, and the lot date of 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 product label for the lot date of October 17, 2013 or later. If you have the product, you may want to contact Good Herbs Inc. for further instructions.
The recall is for quality concerns, not a direct health hazard. There is no risk of injury from using the product.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0292-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0292-2015 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.
