# FDA recall Z-1387-2022

> **SONEX HEALTH LLC** · Class II · device recall initiated 2022-06-29.

## Product

SX-One MicroKnife

## Reason for recall

Potential of dull blade

## Distribution

US Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, ID, IN, KS, MD, MI, MN, MT, NE, NJ, NV, NY, OH, OK, OR, PA, TX, UT, VA, WI, WV, WY.

## Key facts

- **Recall number:** Z-1387-2022
- **Recalling firm:** SONEX HEALTH LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-06-29
- **Report date:** 2022-07-27
- **Termination date:** 2023-04-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Eagan, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1387-2022

## Citation

> AI Analytics. FDA recall Z-1387-2022. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1387-2022. Source: US FDA. Licensed CC0.

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