Trackx Technology Inc: Medical Device Recall in 2023 - (Recall #: Z-1107-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model #605-3TX, Sterile.

Product Classification:

Class II

Date Initiated: October 24, 2022

Date Posted: February 15, 2023

Recall Number: Z-1107-2023

Event ID: 91338

Reason for Recall:

The device is breaking and falling off the Nuvasive T-Handle with Hudson Adapter on certain Nuvasive XLIF instruments during surgery when malleted.

Status: Ongoing

Product Quantity: 464 devices

Code Information:

Insight Base -5L - Lot #2206001, exp. 6/1/2025, UDI 00857088008431; Insight Base 6.5L - Lot #2202002, exp. 2/1/20024, UDI 00857088008448.

Distribution Pattern:

US Nationwide distribution in the states of AZ, FL, LA, NC, PA, VA, WA, WI.

Voluntary or Mandated:

Voluntary: Firm initiated