Good Herbs Inc. recalls multi-herbal 1 oz bottles made on or after Oct 17, 2013 due to not meeting GMP manufacturing standards. Consumers should check product details and contact the company for further information.
Products not manufactured under GMP's
Good Herbs Inc. is recalling their multi-herbal herbal products made on or after October 17, 2013 because they were not manufactured under Good Manufacturing Practices (GMPs). This recall is due to potential quality issues that could affect product safety.
Products not manufactured under GMPs may not meet quality standards, which could lead to potential safety concerns. This means the herbs might not be as pure or effective as advertised, but it does not indicate an immediate risk of injury or illness.
Anyone who purchased Good Herbs Inc.'s multi-herbal herbal products made on or after October 17, 2013. Consumers using these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for the product name 'Multi-herbal', 1 oz bottle, and the manufacturing date of October 17, 2013 or later. The product was distributed by Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084.
Look for the product name 'Multi-herbal', 1 oz bottle, and the manufacturing date of October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could affect product quality and safety.
The official recall notice does not specify a remedy, so contact Good Herbs Inc. for further instructions.
The recall is due to potential quality issues, not an immediate risk of injury or illness.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0352-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0352-2015 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.
