Class II

Medical Device Recall: eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159

Civco Medical Instruments Co. Inc. · March 2, 2026

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.

States Affected

OH, PA, WA

Quantity Affected

21 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1738-2026

Status: ongoing

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