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Medtronic Navigation, Inc. Recalls

56 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Medtronic Navigation, Inc..

56Total Recalls
5Critical
497,793Units Affected
Dec 4, 2024Most Recent
All Recalls

Every Medtronic Navigation, Inc. Recall

Sorted by most recent. Click any recall for full details.

56 recalls
High RiskFDA
Medtronic Navigation, Inc.
TUMOR RESECTION KIT 9733607 NON-INVASIVE
Medical Devices·26,674 affected·Apr 24, 2014
High RiskFDA
Medtronic Navigation, Inc.
SHUNT KIT 9733605 NON-INVASIVE
Medical Devices·26,674 affected·Apr 24, 2014
High RiskFDA
Medtronic Navigation, Inc.
INSTRUMENT TRACKER 9733533XOM ENT 1PK
Medical Devices·26,674 affected·Apr 24, 2014
High RiskFDA
Medtronic Navigation, Inc.
DISP 9730950 STRL SPHERE, 1 PK INSERT
Medical Devices·26,674 affected·Apr 24, 2014
High RiskFDA
Medtronic Navigation, Inc.
Medtronic O-arm Imaging System Mobile X-ray system. Model No. BI-700-00027 and BI-700-00028 The 0-arm Imaging System is a mobile x-ra...
Medical Devices·449 affected·Jul 25, 2013
High RiskFDA
Medtronic Navigation, Inc.
Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic x-ray system, mobile
Medical Devices·463 affected·Jan 31, 2013
High RiskFDA
Medtronic Navigation, Inc.
The Vertex Max Drill Tube is a component within the Navigated Vertex Max Drill Guide Set (item 9733370). The Navigated Vertex Max Drill ...
Surgical Devices·12 affected·Nov 13, 2012
CriticalFDA
Medtronic Navigation, Inc.
Medtronic O-arm¿ Imaging System. Product Numbers: BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120, BI-700-00027-120R, BI-700-00027...
Medical Devices·17 affected·Jul 11, 2012