Good Herbs Inc. recalls digestive kits made on or after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their kit's production date.
Products not manufactured under GMP's
Good Herbs Inc. is recalling digestive kits produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could mean the products are unsafe for consumption.
Products not manufactured under Good Manufacturing Practices (GMPs) may not meet quality and safety standards. This could lead to potential health risks if the products are consumed.
Anyone who owns or uses a Good Herbs digestive kit made on or after October 17, 2013. People who consume these kits are at risk of potential safety issues.
Check the product's production date. Kits made on or after October 17, 2013 are affected. The product is labeled as 'Good Herbs, Inc., DIGESTIVE KIT'.
Look for the production date on the kit, which should be October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could affect their safety and quality.
Check the production date. If it's October 17, 2013 or later, contact Good Herbs Inc. for further instructions.
The recall is due to potential safety issues from not meeting GMPs, but no specific injury mechanism is described.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0176-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0176-2015 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.