Basic Reset Earth Wash Cleaner Recalled for Lack of FDA Approval
Basic Reset Inc. is recalling 949 bottles of Earth Wash Cleaner 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 involves a situation where use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences. The source text does not report any specific illnesses or injuries, aligning with a moderate severity rating for regulatory non-compliance.
Plain-English summary
Basic Reset Inc. is recalling 949 bottles of Basic Reset Earth Wash Cleaner and Personal Care, 2 fl.oz. bottles. 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 is distributed by Basic Reset in Hendersonville, Tennessee. The recall covers lots 120718, 072518, and 112017. The product was distributed in the United States (including Puerto Rico and U.S. Virgin Islands), Canada, Nigeria, the United Kingdom, Australia, Israel, Hungary, the UAE, Mexico, the Philippines, and Greece.
Consumers should stop using the product and contact Basic Reset Inc. for further instructions.
The recalled product
- Product
- Basic Reset Earth Wash Cleaner and Personal Care, Eco Friendly, Non Toxic, 2 fl.oz. bottle, Distributed by: Basic Reset Hendersonville, TN 37075.
- Manufacturer
- Basic Reset Inc.
- Category
- Drug — Personal Care
- Hazard
- Affected units
- 949
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 (4)
- Lots: 120718
- 072518
- 112017
- 120718
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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