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
- 1,312
- Deaths
- 86
- Injuries
- 598
- Malfunctions
- 628
Reports per year
117
120
424
825
1,29826
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Aortic Valve, Prosthesis, Percutaneously DeliveredNPT854
- Device, Vascular, For Promoting EmbolizationKRD105
- Catheter, Percutaneous, NeurovasculatureQJP80
- Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDWF73
- Ring, AnnuloplastyKRH45
- Pulmonary Valve Prosthesis Percutaneously DeliveredNPV38
- Heart-Valve, Non-Allograft TissueLWR28
- ArthroscopeHRX15
- Device, Monitoring, Intracranial PressureGWM13
- Catheter, Electrode Recording, Or Probe, Electrode RecordingDRF11
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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