Medtronic Mexico S. DE R.L. DE CV
FDA adverse event reports naming Medtronic Mexico S. DE R.L. DE CV as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC MEXICO S. DE R.L. DE CV.
- Total reports
- 9,706
- Deaths
- 575
- Injuries
- 4,349
- Malfunctions
- 4,782
Reports per year
115
416
218
119
5520
20821
18922
24923
49624
3,94225
4,55926
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Aortic Valve, Prosthesis, Percutaneously DeliveredNPT5,156
- Catheter, Electrode Recording, Or Probe, Electrode RecordingDRF982
- Device, Vascular, For Promoting EmbolizationKRD824
- Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDWF517
- Device, Monitoring, Intracranial PressureGWM354
- Catheter, Percutaneous, NeurovasculatureQJP350
- Ring, AnnuloplastyKRH269
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX191
- Catheter, Continuous FlushKRA184
- Pulmonary Valve Prosthesis Percutaneously DeliveredNPV183
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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