Medtronic Navigation, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1007-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.

Product Classification:

Class II

Date Initiated: December 12, 2016

Date Posted: January 18, 2017

Recall Number: Z-1007-2017

Event ID: 76060

Reason for Recall:

Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM Touch N Go Pointer Probe because the patient registration accuracy may compromise navigation accuracy when using the StealthStation¿ System with Touch N Go Pointer Probes for patient registration.

Status: Terminated

Product Quantity: 111 devices

Code Information:

lot number 150626B

Distribution Pattern:

US Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated