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Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156
Recalled April 8, 2026 · FDA recall Z-1735-2026 · Civco Medical Instruments
Hazard
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. · FDA Class II
Units
5 units
Sold at
US States: OH, PA, WA. China.
Description
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.
Product
eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156
Manufacturer(s)
Civco Medical Instruments Co. Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →