MDT Puerto Rico Operations Co
FDA adverse event reports naming MDT Puerto Rico Operations Co as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MDT PUERTO RICO OPERATIONS CO.
- Total reports
- 35,502
- Deaths
- 235
- Injuries
- 24,013
- Malfunctions
- 11,246
Reports per year
6,26412
6,00813
5,16414
4,51415
3,97116
3,44517
2,32018
1,27119
68320
14821
5822
5523
5724
3925
1226
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
- Pump, Infusion, Implanted, ProgrammableLKK31,779
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW1,826
- Stimulator, Electrical, Implantable, For IncontinenceEZW1,054
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY680
- Intestinal StimulatorLNQ84
- Bur, Ear, Nose And ThroatEQJ53
- Appliance, Fixation, Spinal InterlaminalKWP9
- Implanted Subcortical Electrical Stimulator (Motor Disorders)MRU7
- Stimulator, Brain, Implanted, For Behavior ModificationMFR2
- Permanent Pacemaker ElectrodeDTB1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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