Good Herbs Inc. recalls kava and St. John's Wort 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 kava and St. John's Wort bottles made on or after October 17, 2013 because they weren't produced under proper food safety standards. This could mean the products aren't safe for consumption as they might not meet quality requirements.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are food safety standards. This means the products might not meet quality and safety requirements, but the risk of serious harm is low.
People who bought Good Herbs kava or St. John's Wort bottles from October 17, 2013 onward are affected. Those using these products for medicinal purposes may be at higher risk due to potential quality issues.
Check for bottles labeled 'Good Herbs, Inc., KAVA & ST. JOHN'S WORT' with a 1 or 4 oz size. Products distributed on or after October 17, 2013 are affected.
Look for the distribution date on the bottle, which should be October 17, 2013 or later.
The recall states the products were not made under Good Manufacturing Practices, but the risk of serious harm is low. They may not meet quality standards.
Check for bottles labeled 'Good Herbs, Inc., KAVA & ST. JOHN'S WORT' 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. 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-0317-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0317-2015 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.
