Health One Pharmaceuticals recalls Qi Vive 80 Veggie Capsules due to cGMP regulatory violations. Consumers should check product labels for 400mg capsules and serial number 8714.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Qi Vive dietary supplements because they violated food safety regulations. This recall affects products sold with the label '80 Veggie Capsules, 400mg' and serial number 8714.
The product was found to have significant violations of current Good Manufacturing Practices (cGMP) regulations for dietary supplements. These violations could lead to unsafe product quality, but the specific hazard isn't detailed in the recall notice.
Anyone who purchased Qi Vive 80 Veggie Capsules, 400mg with serial number 8714 from a retailer. People taking dietary supplements regularly are most at risk.
Check for the label 'Qi Vive, 80 Veggie Capsules, 400mg' and serial number 8714 on the product packaging.
Look for the label 'Qi Vive, 80 Veggie Capsules, 400mg' and serial number 8714 on the product packaging.
Health One Pharmaceuticals is recalling Qi Vive due to significant violations of cGMP regulations for dietary supplements.
Check the product label for 'Qi Vive, 80 Veggie Capsules, 400mg' and serial number 8714. If it matches, contact Health One Pharmaceuticals for instructions.
The recall states there were cGMP violations, but the specific hazard isn't detailed in the notice. The official notice doesn't mention injury risks.
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-1649-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1649-2015 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.
