Good Herbs Inc. recalls female reproductive health herbal bottles from October 2013 due to failure to meet FDA manufacturing standards. Consumers should check product dates and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling female reproductive health herbal bottles produced on or after October 17, 2013, because they were not made under FDA-approved manufacturing practices. This could mean the products might not be safe or effective.
The products were not manufactured under FDA-approved Good Manufacturing Practices (GMPs), which means they might not meet safety or quality standards. This could lead to ineffective or unsafe products, but the risk of serious harm is not specified in the recall.
Women who purchased Good Herbs female reproductive health herbal bottles from October 17, 2013, onward are likely affected. Those using these products for health purposes may be at slightly higher risk due to potential quality issues.
Check for bottles labeled 'Good Herbs, Inc., FEMALE REPRODUCTIVE HEALTH' with a 1 or 4 oz size. Products distributed on or after October 17, 2013, from the manufacturer's address in Troy, MI are affected.
Look for the distribution date on the bottle label, which should be October 17, 2013 or later.
The products were not manufactured under FDA-approved Good Manufacturing Practices (GMPs), which could affect their safety and effectiveness.
Check for bottles labeled 'Good Herbs, Inc., FEMALE REPRODUCTIVE HEALTH' with a 1 or 4 oz size distributed on or after October 17, 2013.
The recall does not specify a remedy, so contact Good Herbs Inc. directly for further instructions.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0200-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0200-2015 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.
