Good Herbs Inc. recalls AQUAACTIVE powder made after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their product's lot date and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling AQUAACTIVE powder produced on or after October 17, 2013 because it wasn't made under proper Good Manufacturing Practices. This recall is due to potential quality issues that could affect product safety.
The product was not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This could lead to potential quality issues, but the recall does not specify a direct health risk or injury mechanism.
Anyone who purchased AQUAACTIVE powder from Good Herbs Inc. after October 17, 2013. People using the product for herbal supplements are most at risk due to potential quality concerns.
Check the product label for the manufacturer's address: 550 Oliver Dr Troy, MI 48084. The recall applies to all lots distributed on or after October 17, 2013.
Look for the distribution date on the product label; recall applies to items made on or after October 17, 2013.
The product was not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality.
Check the product's distribution date. If it's on or after October 17, 2013, contact Good Herbs Inc. for further instructions.
The recall does not specify a direct health risk or injury mechanism, but the product may have quality issues.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0107-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0107-2015 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.
