Health One Pharmaceuticals recalls Cold Plus II dietary supplements due to cGMP regulatory violations. Consumers should check product labels for 3099 batch number.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Cold Plus II dietary supplements because they violated food safety regulations. This recall affects consumers who bought these supplements and may pose risks related to unsafe manufacturing practices.
The supplements were made in facilities that violated current Good Manufacturing Practices (cGMP) for dietary supplements. This means the products may not be safe or effective as intended, potentially causing health issues.
Anyone who purchased Cold Plus II dietary supplements from retailers. People using these supplements for cold relief may be at risk due to the regulatory violations.
Check the product label for 'Cold Plus II, 30 tablets' and batch number 3099. The recall applies to dietary supplements sold by Health One Pharmaceuticals.
Look for the product name 'Cold Plus II, 3:0 tablets' and batch number 3099 on the label.
Health One Pharmaceuticals is recalling Cold Plus II dietary supplements due to significant violations of cGMP regulations for dietary supplements.
The recall record does not specify a remedy, so check the product label for batch number 3099 and contact Health One Pharmaceuticals for further instructions.
The recall record does not mention any specific safety risks or injuries, only 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-1710-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1710-2015 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.
