Good Herbs Inc. recalls GAS Formula 1 & 4 oz bottles made on or after Oct 17, 2013 for not meeting Good Manufacturing Practices. Consumers should contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling their GAS Formula 1 and 4 oz bottles made on or after October 17, 2013 because they weren't produced under proper Good Manufacturing Practices. This could mean the products aren't safe or consistent as they should be.
The products weren't made under Good Manufacturing Practices (GMPs), which are standards for food safety and quality. This could lead to inconsistent product quality or potential safety issues, but the exact risk isn't specified in the recall.
Anyone who bought Good Herbs GAS Formula 1 or 4 oz bottles made on or after October 17, 2013. People using these products for medicinal purposes may be at higher risk.
Check for the product name 'GAS Formula' on 1 or 4 oz bottles. The recall applies to bottles made on or after October 17, 2013, with the address 550 Oliver Dr Troy, MI 48084.
Look for the product name 'GAS Formula' on 1 or 4 oz bottles made on or after October 17, 2013.
The products weren't manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety and quality.
The recall record doesn't specify a remedy, so contact Good Herbs Inc. for details.
The recall states the products weren't made under GMPs, but doesn't specify if there are safety risks or injuries.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0283-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0283-2015 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.