Class II
Medical Device Recall: eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150
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
6 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1732-2026
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.