---
title: "Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 — FDA record Z-2192-2025 | Is It on Recall"
description: "Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time."
url: https://isitonrecall.com/recall/fda-device-z-2192-2025-phasor-drill-ref-2-70s-3-20l-4-50-5-30-6-35/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35 — FDA record Z-2192-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 21, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
- **Reason**: Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
- **Classification**: Class II
- **Recalling firm**: Phasor Health, LLC
- **Quantity**: 1,064
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2192-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2192-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: B775270S0, B775320L0, B7754500, B7755300, B7756350. Lot: 241002450, 241002530, 241009450, 241009530, 241016450, 241016530, 241023450, 241023530, 241030450, 241030530, 24112027S, 24121827S, 24122727S, 25012227S, 24082832L, 24102332L, 241227450, 241220635, 250122635, 241227530, 250122530. |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: Aug 6, 2025
- **Recall initiation date**: Mar 21, 2025
- **Center classification date**: Jul 29, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2192-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Phasor Health, LLC records](https://isitonrecall.com/brand/phasor-health-llc/)