---
title: "eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159 — FDA record Z-1738-2026 | Is It on Recall"
description: "There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be inc"
url: https://isitonrecall.com/recall/fda-device-z-1738-2026-etrax-needle-sensor-18g-for-aurora-trackers-part-number-667-159/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159 — FDA record Z-1738-2026

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 2, 2026. 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**: eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159
- **Reason**: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- **Classification**: Class II
- **Recalling firm**: Civco Medical Instruments Co. Inc.
- **Quantity**: 21 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1738-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1738-2026%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: 00841436111102; Lot Number: A257459, A252198, A268105, A276632 |

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

## Distribution

US States: OH, PA, WA. China.

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

- [Ohio](https://isitonrecall.com/state/ohio/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Apr 8, 2026
- **Recall initiation date**: Mar 2, 2026
- **Center classification date**: Apr 1, 2026

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-1738-2026%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/)