Health One Pharmaceuticals Recalls Bone Rebuilder Dietary Supplement Tablets
Health One Pharmaceuticals is recalling Bone Rebuilder tablets due to significant violations of dietary supplement manufacturing regulations.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves significant cGMP violations, which fits the criteria for a moderate severity recall involving regulatory non-compliance without reported specific acute injuries.
Plain-English summary
Health One Pharmaceuticals Inc is voluntarily recalling Bone Rebuilder, 120 tablets, due to significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements. The recall involves 1,366 units of the product.
The affected product was distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho. It was also distributed internationally in Hong Kong, Vietnam, China, and Singapore. The product code is 2367.
Consumers who have purchased this product should stop using it and contact Health One Pharmaceuticals Inc for further instructions or a refund.
The recalled product
- Product
- Bone Rebuilder, 120 tablets
- Manufacturer
- Health One Pharmaceuticals Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,366
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 2367
Distribution
Part of a larger recall action
This product is one of 147 recalled by Health One Pharmaceuticals Inc under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 147 products in this recall →Related recalls
Same manufacturer · Health One Pharmaceuticals Inc
See all →- ModerateHealth One Pharmaceuticals Recalls Breathe Free Dietary Supplements
FDA (Food) · 2015-04-08
- ModerateHealth One Pharmaceuticals Recalls O.T.I.V Dietary Supplements
FDA (Food) · 2015-04-08
- ModerateHealth One Pharmaceuticals Recalls Bone Essense Dietary Supplement
FDA (Food) · 2015-04-08
- ModerateHealth One Pharmaceuticals Recalls Cholesterol Formula Due to cGMP Violations
FDA (Food) · 2015-04-08
- ModerateHealth One Pharmaceuticals Recalls Tri-Circulator Dietary Supplement
FDA (Food) · 2015-04-08
Same hazard · cGMP violation
See all →- HighHand Sanitizer Recalled Due to Manufacturing Practice Deviations
FDA (Drugs) · 2023-02-08
- ModeratePyrogenium Homeopathic Remedy Recalled for Manufacturing Process Violations
FDA (Drugs) · 2022-06-22
- ModerateDrug Recall: PAINAID Tablets for Manufacturing Deviations
FDA (Drugs) · 2022-02-09
- ModerateDrug Recall: PEPTIME Energy Caffeine Tablets cGMP Violations
FDA (Drugs) · 2022-02-09
- ModerateCalvin Scott Recalls Diethylpropion Tablets Due to Stability Deviations
FDA (Drugs) · 2020-10-14