Good Herbs Inc. recalls circulatory formula bottles from 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 circulatory formula bottles produced on or after October 17, 2013, because they were not made under Good Manufacturing Practices. This recall is important because products not meeting these standards could be unsafe.
The recall is due to products not being made under Good Manufacturing Practices (GMPs). This means the products might not meet safety and quality standards, potentially leading to unsafe ingredients or contamination. However, the hazard does not specify a risk of serious injury or death.
People who bought Good Herbs Circulatory Formula bottles from October 17, 2013, onward are affected. Those using herbal supplements for health purposes may be at risk if the product was not manufactured under proper quality controls.
Check for the product name 'Circulatory Formula' in 1 or 4 oz bottles. The recall applies to all lots distributed on or after October 17, 2013.
Look for the distribution date on the bottle, which should be October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could affect safety and quality.
Check the distribution date on the bottle. If it's October 17, 2013 or later, contact Good Herbs Inc. for further instructions.
The recall does not mention a risk of serious injury or death, so the danger level is low risk.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0163-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0163-2015 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.
