Medtronic MED REL, Inc.
FDA adverse event reports naming Medtronic MED REL, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC MED REL, INC..
- Total reports
- 31,021
- Deaths
- 3,390
- Injuries
- 20,769
- Malfunctions
- 6,787
Reports per year
10599
21700
20301
28002
34403
31204
21805
44606
57607
78608
1,92709
7,36610
9,67211
8,35312
116
Source: FDA adverse event reports by year received, 1999–2016. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Cardioverter Defibrillator (Non-Crt)LWS9,325
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK8,488
- Implantable Pacemaker Pulse-GeneratorDXY7,838
- Pulse Generator, Permanent, ImplantableNVZ3,989
- Detector And Alarm, ArrhythmiaDSI1,023
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP330
- Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)MXC14
- Permanent Pacemaker ElectrodeDTB6
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY2
- Stimulator, Electrical, Implantable, For IncontinenceEZW1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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