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Medtronic Navigation, Inc.: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there were 5 medical device recalls made by Medtronic Navigation, Inc. in 2020. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
  • NavLock Tracker *** Rx Only
  • Mazor X Surgical System Positioner Type II, REF: ASM0214-02
  • Medtronic Nexframe Stereotactic System and StealthStation Cranial software version 3.0 or newer with StealthStation DBS License or StealthStation S8 Software with Stealth DBS License and O-arm Imaging System utilizing the auto-registration (fiducial- less) workflow used in combination during a DBS (deep brain stimulation) procedure. Neurological stereotaxic Instrument.
  • StealthStation" S7 System with Polaris Spectra Camera part number PSU 9733437 - Product Usage: are intended as an aid for precisely locating anatomical structures in either open or percutaneous procedures.
  • Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm catheter VCLAS 9735560, 10mm tip/1.65mm catheter VCLAS 9735561, 15mm tip/1.85mm catheter
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