Health One Pharmaceuticals recalls Lecithin 300 dietary supplements due to significant cGMP regulatory violations. Consumers should check product codes 112114, 112172, 122280, or 122354 for affected items.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Lecithin 300 dietary supplements because they violated food safety regulations. This recall is due to significant violations of current Good Manufacturing Practices (cGMP) for dietary supplements, which could affect product safety.
The recall is triggered by significant violations of current Good Manufacturing Practices (cGMP) for dietary supplements. These violations could lead to unsafe product quality, but the specific hazard mechanism isn't detailed in the recall notice.
Dietary supplement users who purchased Lecithin 300 with product codes 112114, 112172, 122280, or 122354 are likely affected. People who regularly take dietary supplements may be at higher risk due to the regulatory violations.
Check the product code on the label: 112114, 112172, 122280, or 122354. The product is sold as Lecithin 300 dietary supplements by Health One Pharmaceuticals.
Look for product codes 112114, 112172, 122280, or 122354 on the label.
Health One Pharmaceuticals is recalling Lecithin 300 due to significant violations of current Good Manufacturing Practices (cGMP) for dietary supplements.
Product codes 112114, 112172, 122280, and 122354 are affected.
The recall notice does not specify a stop-use instruction; check the product code to determine if it's affected.
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-1731-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1731-2015 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.
