Health One Pharmaceuticals recalls Vigerect dietary supplements due to significant cGMP regulatory violations. Consumers should check product labels for the 8523 model.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Viger: 8523 dietary supplements because they were made without following proper food safety regulations. This could lead to unsafe products being consumed.
The supplements were made without following proper food safety regulations, which could result in unsafe products. This violates the current cGMP (current Good Manufacturing Practices) regulations for dietary supplements.
People who bought the Vigerect dietary supplement labeled '8523' from Health One Pharmaceuticals are affected. Those who have used the product are at risk of consuming unsafe supplements.
Check the product label for the model number '8523'. The product is sold by Health One Pharmaceuticals.
Look for the model number '8523' on the supplement packaging.
The official recall notice states that the product was made without following proper food safety regulations, so it is not safe to use.
Check the product label for the model number '8523' on the Health One Pharmaceuticals Vigerect supplement.
The recall notice does not specify a remedy, so the official notice does not say what to do.
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-1773-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1773-2015 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.