Health One Pharmaceuticals is recalling Lucid-Head dietary supplements because of significant violations of cGMP regulations for dietary supplements. This recall does not specify a specific hazard or remedy.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Lucid:Head dietary supplements due to significant violations of cGMP regulations. This recall indicates potential safety issues with the supplements' manufacturing process.
The recall is based on Health One Pharmaceuticals violating cGMP regulations for dietary supplements. These violations could lead to unsafe products that may pose health risks to consumers.
Dietary supplement users who purchased Lucid-Head supplements from Health One Pharmaceuticals. People who have consumed these supplements may be at risk due to the manufacturing violations.
Lucid-Head supplements with the product code 9327. This recall applies to dietary supplements manufactured by Health One Pharmaceuticals.
Look for the product code 9327 on Lucid-Head supplements to confirm if they are affected.
Health One Pharmaceuticals is recalling Lucid-Head due to significant violations of cGMP regulations for dietary supplements.
Check the product code 9327 to confirm if your supplements are affected. The recall does not specify a remedy.
The recall does not describe a specific hazard, only that Health One Pharmaceuticals violated cGMP regulations.
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-1678-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1678-2015 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.
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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.