Basic Reset Recalls GH-C Dietary Supplement for CGMP Violations
Basic Reset Inc. is recalling GH-C dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was shipped to all 50 states and several foreign countries.
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 due to CGMP violations. Per the rubric, this falls under 'voluntary precautionary recalls' or minor regulatory non-compliance without reported serious injury or death, aligning with a Moderate severity score.
Plain-English summary
Basic Reset Inc. is voluntarily recalling GH-C, a dietary supplement sold in 60-capsule plastic bottles (SKU: 100-4F). The recall was initiated because the products do not conform to Dietary Supplement Current Good Manufacturing Practice (CGMP) regulations.
The affected product was shipped to all 50 states. It was also shipped to foreign consignees in Canada, Nigeria, the U.K., Australia, Israel, Puerto Rico, the Virgin Islands, Hungary, the UAE, Mexico, the Philippines, and Greece. The specific lot codes identified in the recall are 71917 and GH7-17.
Consumers who purchased this product should stop using it and contact Basic Reset Inc. for further instructions. The FDA classifies this recall as Class II, indicating that violation of CGMP regulations may cause temporary or medically reversible health consequences.
The recalled product
- Product
- GH-C, 60 capsules per plastic bottle, SKU: 100-4F
- Manufacturer
- Basic Reset Inc.
- Category
- Food — Dietary Supplement
- Hazard
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 (2)
- 71917
- GH7-17
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 14 recalled by Basic Reset 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.
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