Health One Pharmaceuticals recalls Innoslim dietary supplements due to significant cGMP violations. Consumers should check product labels for 60-capsule units with lot number 8556.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Innos: 60-capsule dietary supplements because they were made without following proper food safety regulations. This recall is due to significant violations of current Good Manufacturing Practices (cGMP) for dietary supplements.
The supplements were made without following proper food safety regulations. This means the product may not be safe for consumption and could cause health issues.
People who own or use Innoslim dietary supplements with lot number 8556 are affected. Those who have taken the product without verifying the lot number are at risk.
Check for Innoslim 60-capsule units with lot number 8556 on the label. The product code 8556 is listed on the packaging.
Look for the lot number 8556 on the Innoslim 60-capsule packaging.
Health One Pharmaceuticals is recalling Innoslim due to significant violations of cGMP regulations for dietary supplements.
Check the product label for lot number 8556. If you have it, you should stop using it and contact Health One Pharmaceuticals for further instructions.
The recall is due to cGMP violations, which may affect product safety, but the official notice does not specify a risk of serious 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-1724-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1724-2015 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.
