# FDA recall Z-1735-2026

> **Civco Medical Instruments Co. Inc.** · Class II · device recall initiated 2026-03-02.

## Product

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

## Reason for recall

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.

## Distribution

US States: OH, PA, WA. China.

## Key facts

- **Recall number:** Z-1735-2026
- **Recalling firm:** Civco Medical Instruments Co. Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-02
- **Report date:** 2026-04-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kalona, IA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1735-2026

## Citation

> AI Analytics. FDA recall Z-1735-2026. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-1735-2026. Source: US FDA. Licensed CC0.

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