Health One Pharmaceuticals recalls 120 vegetarian glucosamine chondroitin MSM capsules due to cGMP regulatory violations. Consumers should check product codes 8663 or 8612 for affected items.
Health One Pharmaceuticals is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Health One Pharmaceuticals is recalling 120 vegetarian glucos:amino chondroitin MSM capsules because they violated food safety regulations. This recall affects products with codes 8663 or 8612.
The product was found to have significant violations of current Good Manufacturing Practices (cGMP) for dietary supplements. These violations could lead to unsafe supplement quality, though the specific risk isn't detailed in the recall.
People who purchased Health One's glucosamine chondroitin MSM capsules with codes 8663 or 8612 are affected. Those using dietary supplements for joint health may be at risk.
Check the product code on the capsule packaging; affected items have codes 8663 or 8612. The product name is 'Glucosamine Chondroitin MSM, 120 Vegetarian Capsules'.
Look for product codes 8663 or 8612 on the capsule packaging to confirm if it's affected.
Health One Pharmaceuticals is recalling these capsules due to significant violations of cGMP regulations for dietary supplements.
Check the product code on the packaging; if it's 8663 or 8612, contact Health One Pharmaceuticals for instructions.
The recall states there were cGMP violations, but the specific hazard isn't detailed in the official notice.
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-1652-2015 — Health One Pharmaceuticals Health One Pharmaceuticals Hello, I own a Health One Pharmaceuticals that is covered by recall F-1652-2015 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.
