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
- 1,581
- Deaths
- 46
- Injuries
- 926
- Malfunctions
- 609
Reports per year
2012
14213
9414
4415
3316
4117
4718
2219
5520
3621
622
1023
1824
26525
30026
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 ReliefLGW381
- Thoracolumbosacral Pedicle Screw SystemNKB251
- Pulse Generator, Permanent, ImplantableNVZ232
- Appliance, Fixation, Spinal InterlaminalKWP206
- 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 IncontinenceEZW29
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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