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
- 9,217
- Deaths
- 547
- Injuries
- 4,144
- Malfunctions
- 4,526
Reports per year
115
416
218
319
5620
20921
18822
25023
49224
3,94225
4,07026
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Aortic Valve, Prosthesis, Percutaneously DeliveredNPT4,899
- Catheter, Electrode Recording, Or Probe, Electrode RecordingDRF979
- Device, Vascular, For Promoting EmbolizationKRD792
- Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDWF488
- Device, Monitoring, Intracranial PressureGWM349
- Catheter, Percutaneous, NeurovasculatureQJP325
- Ring, AnnuloplastyKRH238
- Catheter, Continuous FlushKRA179
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX176
- Pulmonary Valve Prosthesis Percutaneously DeliveredNPV164
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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