Health One Pharmaceuticals recalls Ant Essence dietary supplements due to significant cGMP regulatory violations. Consumers should check product labels for the 7996 model number.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Ant Essence dietary supplements because they violated food safety regulations. This recall affects consumers who bought these supplements and may pose risks from improper manufacturing practices.
The supplements were made without following proper food safety regulations, which could lead to harmful ingredients or contamination. This violation of cGMP (current Good Manufacturing Practices) for dietary supplements means the product may not be safe for consumption.
Anyone who purchased Ant Essence dietary supplements with the model number 7996 from Health One Pharmaceuticals. Consumers who use dietary supplements regularly are most at risk.
Check the product label for the model number 799: 7996. This product was sold by Health One Pharmaceuticals.
Look for the model number 7996 on the product label to confirm if it is recalled.
The official recall notice states that Health One Pharmaceuticals is recalling these supplements due to significant cGMP violations, but it does not specify if they are safe to use.
Check the product label for the model number 7996, as this is the specific product recalled by Health One Pharmaceuticals.
The recall notice does not provide specific action steps for consumers, only that the product is being recalled due to regulatory violations.
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-1694-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1694-2015 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.
