---
title: "VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX — FDA record Z-0395-2022 | Is It on Recall"
description: "There is potential that the VirtuTRAX device will not tighten onto the instrument to be used."
url: https://isitonrecall.com/recall/fda-device-z-0395-2022-virtutrax-instrument-navigator-sensor-with-14-ga-virtuttrax/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX — FDA record Z-0395-2022

Reported terminated

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 Oct 8, 2021. 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**: VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX
- **Reason**: There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
- **Classification**: Class II
- **Recalling firm**: Civco Medical Instruments Co. Inc.
- **Quantity**: 52 boxes (5 units/box)
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0395-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0395-2022%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 | Part Number 5350925; UDI 00841436100892; Lot Numbers: A117795, A119539, A121993, A129844, A131074, A131075, A131690, A142178 |

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

## Distribution

Worldwide distribution - US Nationwide and the countries of Belgium, Canada, China (Mainland), China (Taiwan), Denmark, France, Germany, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Thailand.

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

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## Dates in the source

- **Report date**: Dec 29, 2021
- **Recall initiation date**: Oct 8, 2021
- **Center classification date**: Dec 20, 2021
- **Termination date**: Sep 30, 2024

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-0395-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Civco Medical Instruments Co. Inc. records](https://isitonrecall.com/brand/civco-medical-instruments-co-inc/)
