# FDA recall F-0175-2020

> **Basic Reset Inc.** · Class II · food recall initiated 2019-09-23.

## Product

Ionyte  4 fl. oz. plastic bottle,  SKU: 100-1B

## Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

## Distribution

Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto Rico.

## Key facts

- **Recall number:** F-0175-2020
- **Recalling firm:** Basic Reset Inc.
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2019-09-23
- **Report date:** 2019-11-27
- **Termination date:** 2020-08-19

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Hendersonville, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0175-2020

## Citation

> AI Analytics. FDA recall F-0175-2020. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/F-0175-2020. Source: US FDA. Licensed CC0.

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