Medtronic Puerto Rico Operations Co., Juncos
FDA adverse event reports naming Medtronic Puerto Rico Operations Co., Juncos as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS.
- Total reports
- 2,891
- Deaths
- 49
- Injuries
- 1,327
- Malfunctions
- 1,507
Reports per year
31112
8313
3314
1115
1116
417
418
219
420
221
222
323
424
725
226
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 ReliefLGW914
- Pump, Infusion, Implanted, ProgrammableLKK577
- Stimulator, Electrical, Implantable, For IncontinenceEZW424
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY299
- Pump, Infusion, Insulin, To Be Used With Invasive Glucose SensorOYC220
- Sensor, Glucose, InvasiveMDS138
- Pump, Infusion, InsulinLZG73
- Pulse Generator, Permanent, ImplantableNVZ51
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK45
- Pump, InfusionFRN44
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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