Official recall notice
FDA DeviceClass IINotable
FDA Recall: eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159
- Recall date
- 2026-04-08
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
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.
Recommended action
What to do
21 units
Product 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.