Good Herbs Inc. recalls RHODIOLA 1 oz bottles made on or after Oct 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check product details and contact the company for guidance.
Products not manufactured under GMP's
Good Herbs Inc. is recalling RHODIOLA herbal supplements made on or after October 17, 2013 because they were not produced under Good Manufacturing Practices. This recall is due to potential quality issues that could affect product safety.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product quality and safety. This could mean the supplements might not be as safe or effective as intended, but the recall does not specify a risk of serious injury.
Anyone who owns or uses Good Herbs Inc. RHODIOLA herbal supplements made on or after October 17, 2013. People using these products for health purposes may be at risk if the supplements do not meet quality standards.
Check for the product name 'RHODIOLA', 1 oz bottle, and the manufacturing date of October 17, 2013 or later. The products were distributed by Good Herbs Inc. from their Troy, MI address.
Look for the product name 'RHODIOLA', 1 oz bottle, and the manufacturing date of October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product quality and safety.
The recall does not specify a remedy, so contact Good Herbs Inc. for guidance on next steps.
The products were distributed on or after October 17, 2013.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0398-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0398-2015 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.
