Health One Pharmaceuticals is recalling Ashitaba dietary supplements after significant violations of cGMP regulations for dietary supplements. Consumers should check product labels for the recall.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Ashit: a dietary supplement product due to significant violations of cGMP regulations. This recall is necessary to address potential safety risks associated with the product.
The recall is due to significant violations of cGMP regulations for dietary supplements. These violations could lead to safety risks, but the specific hazard mechanism is not clearly described in the recall notice.
Anyone who purchased Ashitaba dietary supplements from Health One Pharmaceuticals. Consumers who use dietary supplements are most at risk.
Check product labels for the name 'Ashitaba'. The product was sold by Health One Pharmaceuticals Inc. No specific model numbers or dates are provided in the recall notice.
Look for the product name 'Ashitaba' on the label to confirm if it is part of the recall.
Health One Pharmaceuticals is recalling Ashitaba due to significant violations of cGMP regulations for dietary supplements.
Check the product label for 'Ashitaba' to confirm if it is part of the recall. No specific remedy is provided in the recall notice.
The recall notice states significant violations of cGMP regulations, but does not specify the exact hazard or risk of injury.
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-1697-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1697-2015 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.
