Class II

Medical Device Recall: eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152

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

20 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1734-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Civco Medical Instruments Co. Inc. Medical Device Recall: eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152 | SafeCheck