Medtronic Puerto Rico Operations Med-rel
FDA adverse event reports naming Medtronic Puerto Rico Operations Med-rel as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC PUERTO RICO OPERATIONS MED-REL.
- Total reports
- 10,678
- Deaths
- 239
- Injuries
- 6,388
- Malfunctions
- 4,038
Reports per year
5306
58807
95908
2,55609
3,58610
2,93611
Source: FDA adverse event reports by year received, 2006–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, Infusion, InsulinLZG5,897
- Sensor, Glucose, InvasiveMDS3,545
- Syringe, PistonFMF564
- Pump, InfusionFRN532
- Pump, Infusion, Insulin, To Be Used With Invasive Glucose SensorOYC109
- Glucose Oxidase, GlucoseCGA24
- Warmer, Thermal, Infusion FluidLGZ3
- Stimulator, Electrical, Implantable, For IncontinenceEZW1
- Product code LGTLGT1
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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