Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
- Recall date
- March 2, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1731-2026
- 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 System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
Get recall alerts
Free email alert whenever Civco Medical Instruments Co. Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Civco Medical Instruments Co. Inc.