Health One Pharmaceuticals recalls SOD Herbal Mix due to significant cGMP regulatory violations in dietary supplements. Consumers should check product labels for the 8939 model.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling their SOD Herbal Mix dietary supplement because it was made without following proper food safety regulations. This recall is due to significant violations of current Good Manufacturing Practices (cGMP) for dietary supplements.
The product was made without following proper food safety regulations, which means it may not be safe for consumption. This is a violation of current Good Manufacturing Practices (cGMP) for dietary supplements.
People who purchased the SOD Herbal Mix dietary supplement from Health One Pharmaceuticals are affected. Those who have the product are at risk due to the regulatory violations.
Check the product label for the model number 8939. The product is sold by Health One Pharmaceuticals.
Look for the model number 8939 on the SOD Herbal Mix product.
Health One Pharmaceuticals is recalling SOD Herbal Mix due to significant violations of cGMP regulations for dietary supplements.
The recall record does not specify a remedy, so check the product label for the model number 8939 and contact Health One Pharmaceuticals for further instructions.
The recall record does not mention any specific safety hazards, so the risk 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-1683-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1683-2015 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.
