Health One Pharmaceuticals recalls Suth: 9496 dietary supplements due to cGMP regulatory violations. Consumers should check product labels for this specific capsule model.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling a dietary supplement capsule called SutharIndia (model 9496) because it was made without following proper food safety regulations. This recall is due to significant violations of current Good Manufacturing Practices for dietary supplements.
The product was made without following proper food safety regulations, which could lead to unsafe levels of ingredients. This violates the current Good Manufacturing Practices for dietary supplements, meaning the product might not be safe for consumption.
Anyone who purchased the SutharIndia capsule (model 9496) from Health One Pharmaceuticals. People who take dietary supplements regularly are most at risk.
Check for the product name 'SutharIndia' and model number '9496' on the capsule label. The recall applies to dietary supplements sold by Health One Pharmaceuticals.
Look for the product name 'SutharIndia' and model number '9496' on the capsule label.
Health One Pharmaceuticals is recalling the SutharIndia capsule (model 9496) due to significant violations of current Good Manufacturing Practices for dietary supplements.
The recall record does not specify a remedy or action for consumers.
The recall record does not describe any specific injury risk or hazard mechanism.
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-1630-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1630-2015 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.
