Good Herbs Inc. recalls LVGL capsules made on or after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their capsules for the lot date and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling LVGL capsules produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could affect product safety and quality.
The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This means the capsules might not meet the expected quality and safety standards for herbal supplements.
People who purchased Good Herbs LVGL capsules made on or after October 17, 2013 are affected. Those using these capsules for herbal supplements may be at risk if the product does not meet quality standards.
Check for the lot date on the capsule packaging. Products distributed on or after October 17, 2013 are affected. The product name is LVGL capsules from Good Herbs Inc.
Look for the lot date on the capsule packaging to determine if it was made on or after October 17, 2013.
The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality.
Check the lot date on the packaging. If made on or after October 17, 2013, contact Good Herbs Inc. for further instructions.
The recall is due to not meeting quality standards, but specific health risks are not detailed in the official notice.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0335-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0335-2015 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.