Health One Pharmaceuticals recalls Super Gan: dietary supplements with cGMP violations. Consumers should check product labels for 8670 and contact for details.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Super Ganoderma dietary supplements due to significant violations of cGMP regulations. This recall affects consumers who may have purchased these supplements and could pose risks related to product safety.
The recall is due to significant violations of cGMP regulations for dietary supplements. These violations could lead to unsafe products that may not meet quality standards, though specific hazards like contamination or harmful ingredients are not detailed in the notice.
Anyone who purchased Super Ganoderma dietary supplements labeled '8670' from Health One Pharmaceuticals. Consumers using these supplements are at risk due to regulatory violations.
Check for the product name 'Super Ganoderma' and the model number '8670' on the label. This recall applies to products sold by Health One Pharmaceuticals.
Look for the model number '8670' on the Super Ganoderma supplement label.
Health One Pharmaceuticals is recalling Super Ganoderma due to significant violations of cGMP regulations for dietary supplements.
The recall record does not specify a remedy, so check the product label for model number '8670' and contact Health One Pharmaceuticals for further instructions.
The recall record does not describe specific hazards like injury or illness, only regulatory violations.
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-1763-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1763-2015 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.
