Health One Pharmaceuticals recalls Lutimax dietary supplements due to significant cGMP regulatory violations. Consumers should check product labels for 2362 and contact the company for details.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Lut:imax dietary supplements because they violated food safety regulations. This recall affects consumers who bought these supplements and may pose risks related to product safety.
The supplements were made without following proper food safety regulations. This could lead to unsafe products that might harm consumers if they cause health issues.
Anyone who purchased Lutimax dietary supplements from Health One Pharmaceuticals. People using these supplements for health purposes are most at risk due to regulatory violations.
Check for the product name 'Lutimax' and the code '2362' on the label. The recall applies to dietary supplements sold by Health One Pharmaceuticals.
Look for the product name 'Lutimax' and the code '2362' on the label.
Health One Pharmaceuticals is recalling Lutimax dietary supplements due to significant violations of cGMP regulations for dietary supplements.
Check for the product name 'Lutimax' and the code '2362' on the label.
The recall does not specify a remedy, so contact Health One Pharmaceuticals for further instructions.
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-1732-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1732-2015 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.
