Health One Pharmaceuticals recalls Liver Best dietary supplements due to cGMP regulatory violations. Consumers should check product labels for 60-capsule bottles with 8955.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Liver Best dietary supplements because they were made without following food safety regulations. This could mean the product is unsafe for consumption.
The supplements were made without following food safety regulations. This means the product could be unsafe for consumption, but the specific health risks aren't clearly stated in the recall notice.
People who bought Liver Best dietary supplements from stores or online. Those who have the product are at risk of consuming unsafe supplements.
Check for Liver Best 60-capsule bottles labeled with 8955. The product was sold by Health One Pharmaceuticals.
Look for the product name 'Liver Best', 60 capsules, and the code 8955 on the label.
The recall states there were significant violations of cGMP regulations, but the specific health risks aren't clearly described in the notice.
The recall does not specify a remedy, so there is no action required beyond checking if you have the product.
Check the product label for 'Liver Best', 60 capsules, and the code 8955.
We’ve drafted a message you can send Health One Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall F-1632-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1632-2015 from Health One Pharmaceuticals. 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.
