Basic Reset Recalls AquaLyte Dietary Supplement for CGMP Violations
Basic Reset Inc. is recalling AquaLyte dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 low probability of serious adverse health consequences. The source text cites a regulatory compliance issue (CGMP) without reporting specific illnesses, injuries, or high-risk pathogens, aligning with the Moderate severity criteria for low-risk or precautionary recalls.
Plain-English summary
Basic Reset Inc. is voluntarily recalling AquaLyte, 30g pkg./foil pouch, SKU: 1023. The recall is being conducted because the products do not conform to Dietary Supplement Current Good Manufacturing Practice (CGMP) regulations. The specific nature of the non-conformance is not detailed in the source text.
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 source text lists Puerto Rico twice in the distribution list.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions. The source text does not specify a lot number, expiration date, or specific health risks associated with the CGMP violation.
The recalled product
- Product
- AquaLyte, 30g pkg./foil pouch, SKU: 1023
- 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 (1)
- 91117
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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