Good Herbs Inc. recalls JUNIPER herbs from October 17, 2013 onward 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 JUNIPER herbal products sold from October 17, 2013, because they were not made under Good Manufacturing Practices. This could mean the products are unsafe for consumption.
Products not made under Good Manufacturing Practices (GMPs) may have unsafe levels of contaminants or impurities. This could lead to health issues if consumed, though the specific risk is not detailed in the recall.
Anyone who bought Good Herbs JUNIPER herbs from October 17, 2013, onward. People using these products for medicinal purposes may be at higher risk due to potential contamination.
Check for the product name 'JUNIPER' and the size (1 or 4 oz) on the label. Products were distributed starting October 17, 2013, from the manufacturer's location in Troy, MI.
Look for the distribution date on the label, which starts from October 17, 2013.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could lead to unsafe levels of contaminants.
Check for the product name 'JUNIPER' and the size (1 or 4 oz) on the label. Products were distributed starting 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-0315-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0315-2015 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
