Good Herbs Inc. recalls 1 & 4 oz herb bottles made on or after October 17, 2013 due to failure to meet Good Manufacturing Practices. Consumers should contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling 1 and 4 ounce herb bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could mean the products don't meet food safety standards, though the recall doesn't specify a risk of injury or illness.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are food safety standards. This means the products might not be safe for consumption, but the recall does not specify a risk of injury or illness.
People who bought Good Herbs Inc. 1 or 4 ounce herb bottles made on or after October 17, 2013 are affected. Those who use these products for food or herbal remedies may be at risk if the products don't meet food safety standards.
Check for Good Herbs Inc. 1 or 4 ounce herb bottles with the address 550 Oliver Dr, Troy, MI 48084. The products were distributed on or after October 17, 2013.
Identify if your bottle was made on or after October 17, 2013 and has the address 550 Oliver Dr, Troy, MI 48084.
The recall states the products were not manufactured under Good Manufacturing Practices, but it does not specify a risk of injury or illness.
Check for Good Herbs Inc. 1 or 4 ounce herb bottles made on or after October 17, 2013 with the address 550 Oliver Dr, Troy, MI 48084.
The recall does not specify a remedy, so contact Good Herbs Inc. for details.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0334-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0334-2015 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.