Basic Reset Recalls Vibrant Energy Drink Pouches for CGMP Violations
Basic Reset Inc. is recalling 6,887 cases of Vibrant Energy Drink 15 g foil pouches because the products do not conform to Dietary Supplement CGMP 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 due to CGMP non-conformance, which typically indicates a reasonable probability of temporary or medically reversible health adverse effects, fitting the Moderate severity criteria for regulatory compliance issues without reported acute illness.
Plain-English summary
Basic Reset Inc. is voluntarily recalling 6,887 cases of Vibrant Energy Drink 15 g foil pouches (15 pack case), specifically codes 100-4A and 100-4B. 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 and 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 associated with the recall are F1246L and P12317.
Consumers who have purchased this product should stop using it and contact Basic Reset Inc. for further instructions or a refund. The recall is classified as FDA Class II, indicating a reasonable probability that use of the product could cause temporary or medically reversible health adverse effects.
The recalled product
- Product
- Vibrant ENERGY DRINK 15 g foil pouches (15 pack case) 100-4A and 100-4B
- Manufacturer
- Basic Reset Inc.
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 6,887
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)
- F1246L and P12317
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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