Basic Reset CBD Oil Recalled for Lack of FDA Approval
Basic Reset Inc. is recalling 598 bottles of CBD Reset 750 True Full Spectrum Cinnamon because the product was marketed without an approved NDA or ANDA.
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 indicates a situation where use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences. The specific hazard is the lack of regulatory approval rather than a specific contamination or injury report.
Plain-English summary
Basic Reset Inc. is recalling 598 bottles of Basic Reset CBD Reset 750 True Full Spectrum Cinnamon, 750 mg CBD, 1 fl. oz. (30 mL) bottles. The product was distributed in the United States (including Puerto Rico and U.S. Virgin Islands), Canada, Nigeria, the United Kingdom, Australia, Israel, Hungary, UAE, Mexico, Philippines, and Greece. The specific lots affected are 1902411.25 and 1916911.25.
The recall was initiated because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). This means the product has not been evaluated by the FDA for safety, efficacy, or quality.
Consumers who have purchased this product should stop using it and contact Basic Reset Inc. for further instructions or a refund.
The recalled product
- Product
- Basic Reset CBD Reset 750 True Full Spectrum Cinnamon, 750 mg CBD, 1 fl. oz. (30 mL) bottle, Distributed by: Basic Reset Hendersonville, TN 37075
- Manufacturer
- Basic Reset Inc.
- Category
- Drug — CBD Product
- Hazard
- Affected units
- 598
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)
- Lots: 1902411.25
- 1916911.25
Distribution
Part of a larger recall action
This product is one of 11 recalled by Basic Reset Inc. under a single FDA (Drugs) 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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