# FDA recall Z-2192-2025

> **Phasor Health, LLC** · Class II · device recall initiated 2025-03-21.

## Product

Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35

## Reason for recall

Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.

## Distribution

US: PA, IN, AZ, MO, LA, FL, TX, MA, OH, TN, MI, WV, VA, CA, DE, NH, GA, SC, GU, NY, NJ, MN, WI, NE, WA, IL, AR, PR, VT

## Key facts

- **Recall number:** Z-2192-2025
- **Recalling firm:** Phasor Health, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-21
- **Report date:** 2025-08-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2192-2025

## Citation

> AI Analytics. FDA recall Z-2192-2025. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2192-2025. Source: US FDA. Licensed CC0.

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