Health One Pharmaceuticals is recalling Ultra Lec: 122278 due to significant cGMP violations in dietary supplements. Consumers should check product labels for the recall number.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Ultra Lecithin 200 dietary supplements because they violated cGMP regulations. This means the product may not be safe for consumption.
The product was made with significant violations of cGMP regulations for dietary supplements. These violations could lead to unsafe ingredients or improper manufacturing practices.
Anyone who owns or uses Ultra Lecithin 200 dietary supplements. People who consume these supplements are at risk due to the regulatory violations.
Check for the product name 'Ultra Lecithin 200' and the recall number 122278 on the label. The product was sold by Health One Pharmaceuticals.
Look for the product name 'Ultra Lecithin 200' and recall number 122278 on the label.
Health One Pharmaceuticals is recalling Ultra Lecithin 200 due to significant violations of cGMP regulations for dietary supplements.
Check the product label for 'Ultra Lecithin 200' and recall number 122278. If you have it, you should stop using it and contact Health One Pharmaceuticals.
The recall record does not mention a remedy or fix for this product.
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-1769-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1769-2015 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.