Health One Pharmaceuticals recalls Shu Chang: Dietary supplements with significant cGMP violations. Consumers should check product labels for 9756 and contact the company 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 Shu Chang Bao_A capsules due to significant violations of cGMP regulations for dietary supplements. This recall affects consumers who may have purchased these supplements, which could pose risks related to product safety and quality.
The recall is due to significant violations of current Good Manufacturing Practices (cGMP) regulations for dietary supplements. These violations could lead to unsafe product quality or potential health risks if the supplements are consumed.
Consumers who purchased Shu Chang Bao_A capsules from Health One Pharmaceuticals are affected. Those who have used these supplements may be at risk due to regulatory violations.
Check for the product name 'Shu Chang Bao_A' and the code '9756' on the label. The recall applies to dietary supplements sold by Health One Pharmaceuticals.
Look for the product name 'Shu Chang Bao_A' and code '9756' on the label.
Health One Pharmaceuticals is recalling these supplements due to significant violations of cGMP regulations for dietary supplements.
The recall record does not specify a remedy, so contact Health One Pharmaceuticals directly for further instructions.
The recall record does not describe specific injury risks, so the hazard level 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-1639-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1639-2015 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.
