Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158
- Recall date
- March 2, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1737-2026
- FDA classification
- Class II
- Brand / firm
- Civco Medical Instruments Co. Inc.
- Sold / distributed
- US States: OH, PA, WA. China.
Why it was 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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158
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