Health One Pharmaceuticals Recalls Gymostemma Capsules for cGMP Violations
Health One Pharmaceuticals is recalling Gymostemma Capsules due to significant violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements.
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, which typically involves a situation where use of, or exposure to, a violative product may cause temporary or medically reversible health consequences. The source text does not report any specific illnesses, injuries, or deaths, and the hazard is related to manufacturing compliance rather than a specific pathogen or allergen.
Plain-English summary
Health One Pharmaceuticals is voluntarily recalling Gymostemma Capsules. The recall is being conducted because the product was found to have significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements.
The recall involves 1,602 units of the product. Distribution was nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho, as well as internationally in Hong Kong, Vietnam, China, and Singapore. The product code associated with the recall is 7882.
Consumers who have purchased Gymostemma Capsules should stop using the product and contact Health One Pharmaceuticals for further instructions or a refund.
The recalled product
- Product
- Gymostemma Capsules
- Manufacturer
- Health One Pharmaceuticals Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,602
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)
- 7882
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