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
- 1,551
- Deaths
- 46
- Injuries
- 909
- Malfunctions
- 596
Reports per year
2012
14213
9414
4415
3316
4117
4718
2219
5520
3621
622
1023
1824
26525
26926
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW382
- Thoracolumbosacral Pedicle Screw SystemNKB242
- Pulse Generator, Permanent, ImplantableNVZ231
- Appliance, Fixation, Spinal InterlaminalKWP196
- Implantable Pacemaker Pulse-GeneratorDXY109
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY97
- Implantable Cardioverter Defibrillator (Non-Crt)LWS65
- Intervertebral Fusion Device With Bone Graft, LumbarMAX64
- Stimulator, Electrical, Implantable, For IncontinenceEZW31
- Bone Cement, Posterior Screw AugmentationPML30
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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