Medtronic Mexico
FDA adverse event reports naming Medtronic Mexico as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC MEXICO.
- Total reports
- 6,360
- Deaths
- 136
- Injuries
- 1,601
- Malfunctions
- 4,623
Reports per year
2812
4813
11714
18615
16916
29717
46718
52019
51920
36221
45222
1,31323
1,26124
61225
626
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX1,730
- Device, Monitoring, Intracranial PressureGWM1,006
- Catheter, Electrode Recording, Or Probe, Electrode RecordingDRF554
- Catheter, Angioplasty, Peripheral, TransluminalLIT503
- Tubing, Pump, Cardiopulmonary BypassDWE433
- Device, Vascular, For Promoting EmbolizationKRD404
- ArthroscopeHRX359
- Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDWF279
- Catheter, PercutaneousDQY245
- Ring, AnnuloplastyKRH234
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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