# FDA recall Z-0348-2020

> **Basic Reset Inc.** · Class II · device recall initiated 2019-10-18.

## Product

Energy FX:  a) original Aluminum (100-3A)   b) sleek (adult and kid & pet) (100-3B)

## Reason for recall

FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.

## Distribution

US, Puerto Rico, U.S. Virgin Islands,  Canada, Mexico, Australia, PHILIPPINES,  Greece, United Kingdom, Israel, Nigeria, Hungary, United Arab Emirates

## Key facts

- **Recall number:** Z-0348-2020
- **Recalling firm:** Basic Reset Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2019-10-18
- **Report date:** 2019-11-20

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0348-2020

## Citation

> AI Analytics. FDA recall Z-0348-2020. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-0348-2020. Source: US FDA. Licensed CC0.

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