Basic Reset CBD Product Recalled for Lack of FDA Approval
Basic Reset Inc. is recalling 391 bottles of CBD Reset 2400 because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (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 typically indicates a situation where use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences. The specific violation is regulatory (lack of approval) rather than a direct physical hazard like contamination.
Plain-English summary
Basic Reset Inc. is recalling 391 bottles of Basic Reset CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD, 1 fl. oz. (29 mL) bottles. The product is identified by Lot 1903011.8. The recall was initiated because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
The affected product was distributed in the United States (including Puerto Rico and U.S. Virgin Islands), Canada, Nigeria, United Kingdom, Australia, Israel, Hungary, UAE, Mexico, Philippines, and Greece.
Consumers who have purchased this product should stop using it and contact Basic Reset Inc. for further instructions.
The recalled product
- Product
- Basic Reset CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD, 1 fl. oz. (29 mL) bottle, Distributed by: Basic Reset Hendersonville, TN 37075
- Manufacturer
- Basic Reset Inc.
- Category
- Drug — CBD Product
- Hazard
- Affected units
- 391
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)
- Lot: 1903011.8
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.
See all 11 products in this recall →Related recalls
Same manufacturer · Basic Reset Inc.
See all →- ModerateBasic Reset Recalls Bee Gold Dietary Supplements for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Ionyte Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Beta Factor Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls AquaLyte Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Vibrant Energy Drink for CGMP Violations
FDA (Food) · 2019-11-27
Same hazard · unapproved drug
See all →- CriticalBuy-Herbal Recalls Kian Pee Wan Capsules for Undeclared Drug Ingredients
FDA (Drugs) · 2026-08-19
- SevereMojo Max Fusion capsules recalled as Class I over undeclared drug ingredients
FDA (Drugs) · 2026-03-11
- SevereMR. 7 Super capsules recalled as Class I over undeclared sildenafil
FDA (Drugs) · 2026-03-11
- SevereSilintan herbal pills recalled as Class I for undeclared meloxicam
FDA (Drugs) · 2026-03-11
- HighChildren's growth supplement recalled for containing undeclared ibutamoren
FDA (Drugs) · 2026-03-04