CLASS II ONGOING Device recall · Reported 8 Apr 2026 · FDA Enforcement Report

eTRAX Needle Sensor - (for Aurora Trackers) recalled

Civco Medical Instruments is recalling eTRAX Needle Sensor - (for Aurora Trackers), distributed in Ohio, Pennsylvania, Washington. The recall was initiated on 2 Mar 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI-DI: 00841436111072; Lot Number: A276634
Quantity recalled5 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1735-2026
FDA event ID
98513
Recalling firm
Civco Medical Instruments, Kalona, IA
Classification
Class II
Status
Ongoing
Recall initiated
2 Mar 2026
FDA classified
1 Apr 2026
Reported
8 Apr 2026
Type
Voluntary: Firm initiated
Reason category
Processing Deviation

Timeline

2 Mar 2026Recall initiated by company
1 Apr 2026Classified by FDA+30 days
8 Apr 2026Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

The USDA issues these when meat or poultry was produced without proper inspection, or when a step such as cooking or pasteurisation did not meet requirements.

Product as listed by the FDA

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

Where it was distributed

US States: OH, PA, WA. China.

OhioPennsylvaniaWashington

Questions about this recall

Why was it recalled?

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.

Which lots are affected?

UDI-DI: 00841436111072; Lot Number: A276634

Where was it sold?

US States: OH, PA, WA. China.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

7 other products · FDA event 98513

This product is part of a recall event; the main page for the event is eTRAX Needle System Starter Kit (for Aurora Trackers) recalled.

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