Medical Device

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

Recall date: 2026-04-08 · Source: FDA_DEVICE

Brand / Firm

Product

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.

Units affected

5 units

Description

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

View official recall notice →