Health One Pharmaceuticals recalls Bene-X dietary supplements due to significant cGMP regulatory violations. Consumers should check product labels for 2265.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling Bene-X dietary supplements because they violated cGMP regulations for dietary supplements. This recall affects consumers who purchased these products from authorized retailers.
The supplements were produced under significant violations of current Good Manufacturing Practices (cGMP) regulations. These violations could lead to unsafe products that may not meet quality standards. The specific risks are not detailed in the recall notice.
Anyone who purchased Bene-X dietary supplements with the model number 2265 from authorized retailers. Consumers who use dietary supplements are most at risk due to regulatory violations.
Check the product label for the model number 2265. The product name is Bene-X. This recall applies to dietary supplements sold by Health One Pharmaceuticals.
Look for the model number 2265 on the product label to confirm if it is affected.
Health One Pharmaceuticals is recalling Bene-X dietary supplements due to significant violations of cGMP regulations for dietary supplements.
Check the product label for the model number 2265. The product name is Bene-X.
The recall notice does not specify a remedy or action for affected consumers.
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-1700-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1700-2015 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.
