MDT Puerto Rico Operations Co, MED REL
FDA adverse event reports naming MDT Puerto Rico Operations Co, MED REL as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MDT PUERTO RICO OPERATIONS CO, MED REL.
- Total reports
- 1,583
- Deaths
- 46
- Injuries
- 927
- Malfunctions
- 610
Reports per year
2012
14213
9414
4415
3316
4117
4718
2219
5520
3621
622
1023
1924
26525
30126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW382
- Thoracolumbosacral Pedicle Screw SystemNKB252
- Pulse Generator, Permanent, ImplantableNVZ232
- Appliance, Fixation, Spinal InterlaminalKWP205
- Implantable Pacemaker Pulse-GeneratorDXY109
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY98
- Intervertebral Fusion Device With Bone Graft, LumbarMAX69
- Implantable Cardioverter Defibrillator (Non-Crt)LWS65
- Bone Cement, Posterior Screw AugmentationPML35
- Stimulator, Electrical, Implantable, For IncontinenceEZW30
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor MDT Puerto Rico Operations Co, MED REL 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.