Medtronic MED REL Medtronic Puerto Rico
FDA adverse event reports naming Medtronic MED REL Medtronic Puerto Rico as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC MED REL MEDTRONIC PUERTO RICO.
- Total reports
- 88,058
- Deaths
- 1,205
- Injuries
- 48,588
- Malfunctions
- 38,264
Reports per year
8911
6,38312
18,18113
16,63814
12,07015
9,27516
7,02317
5,63718
3,73019
2,60820
1,80221
1,51922
1,60923
1,07924
32025
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW33,759
- Stimulator, Electrical, Implantable, For IncontinenceEZW16,485
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK8,809
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY8,310
- Implantable Cardioverter Defibrillator (Non-Crt)LWS8,110
- Pulse Generator, Permanent, ImplantableNVZ7,863
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP1,417
- Intestinal StimulatorLNQ1,103
- Detector And Alarm, ArrhythmiaDSI857
- Implanted Subcortical Electrical Stimulator (Motor Disorders)MRU704
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Medtronic MED REL Medtronic Puerto Rico automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.