Medtronic Navigation, Inc. (louisville)
FDA adverse event reports naming Medtronic Navigation, Inc. (louisville) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC NAVIGATION, INC. (LOUISVILLE).
- Total reports
- 8,331
- Deaths
- 31
- Injuries
- 703
- Malfunctions
- 7,597
Reports per year
93915
1,75716
2,86017
2,76218
1219
120
Source: FDA adverse event reports by year received, 2015–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Neurological Stereotaxic InstrumentHAW7,032
- Orthopedic Stereotaxic InstrumentOLO917
- Powered Laser Surgical InstrumentGEX246
- Ear, Nose, And Throat Stereotaxic InstrumentPGW101
- Image-Intensified Fluoroscopic X-Ray System, MobileOXO19
- Interventional Fluoroscopic X-Ray SystemOWB7
- Instrument, Surgical, Non-PoweredHAO4
- System, Nuclear Magnetic Resonance ImagingLNH2
- Cart, Emergency, Cardiopulmonary (Excluding Equipment)BZN1
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Medtronic Navigation, Inc. (louisville) automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.