Health One Pharmaceuticals recalls Ultra Lec: Dietary supplements with significant cGMP violations. Consumers should check product labels for 112121.
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 dietary supplements due to significant violations of current Good Manufacturing Practices (cGMP) regulations. This recall affects consumers who may have purchased the product, though the specific risk to health is not detailed in the notice.
The recall is based on Health One Pharmaceuticals violating cGMP regulations for dietary supplements. These violations could potentially lead to unsafe products, but the specific hazard mechanism is not described in the notice.
Consumers who purchased Ultra Lecithin dietary supplements with the label '112121' are likely affected. The recall does not specify which individuals are at higher risk.
Check the product label for 'Ultra Lecithin' and the code '112121'. The recall does not specify when or where the product was sold.
Look for the label 'Ultra Lecithin' and the code '112121' on the product.
Health One Pharmaceuticals is recalling Ultra Lecithin due to significant violations of cGMP regulations for dietary supplements.
The recall does not specify a remedy, so check the product label for 'Ultra Lecithin' and code '112121' to confirm if it's affected.
The recall does not describe a specific hazard mechanism, so the risk to health is unknown.
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-1768-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1768-2015 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.
