Health One Pharmaceuticals recalls Anti-u Allergies dietary supplements due to significant cGMP regulatory violations. Consumers should check product labels for 9226 model.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Anti-u Allergies dietary supplements because they violated food safety regulations. This recall affects products labeled '9226' and may pose risks from improper manufacturing.
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, but the specific hazard isn't detailed in the notice.
Anyone who owns or uses the Anti-u Allergies dietary supplement labeled '9226' is affected. People with allergies or sensitive health conditions may be at higher risk.
Check the product label for the model number '9226'. The product name is 'Anti-u Allergies'. This recall applies to dietary supplements sold by Health One Pharmaceuticals.
Look for the model number '9226' on the supplement packaging.
Health One Pharmaceuticals is recalling Anti-u Allergies dietary supplements due to significant violations of cGMP regulations for dietary supplements.
The recall notice does not specify a remedy or action steps beyond checking the product label for model number '9226'.
The recall notice does not describe a specific hazard mechanism or risk of 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-1695-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1695-2015 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.
