Health One Pharmaceuticals recalls Stem Alive dietary supplements due to cGMP regulatory violations. Consumers should check product labels for 90-capsule units with batch 8671.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Stem Alive dietary supplements because they were made without following proper food safety regulations. This recall affects people who bought these supplements and could pose risks to their health.
The supplements were made without following proper food safety regulations, which could lead to harmful ingredients or incorrect dosing. This violates the current good manufacturing practices required for dietary supplements.
People who bought Stem Alive dietary supplements containing 90 capsules with batch number 8671 are affected. Those who took the supplements without checking the batch number may be at risk.
Check for the product name 'Stem Alive' and the batch number 8671 on the label. The product is sold as 90 capsules.
Look for the batch number 8671 on the Stem Alive supplement label.
The official recall notice states that the supplements were made without following proper food safety regulations, so they are not safe to use.
Check for the product name 'Stem Alive' and batch number 8671 on the label.
The recall notice does not specify a remedy, so you should check with Health One Pharmaceuticals for further instructions.
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-1760-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1760-2015 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.
