Medtronic Dominicana
FDA adverse event reports naming Medtronic Dominicana as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC DOMINICANA.
- Total reports
- 1,780
- Deaths
- 15
- Injuries
- 333
- Malfunctions
- 1,432
Reports per year
120
422
1123
45824
88925
41726
Source: FDA adverse event reports by year received, 2020–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Stimulator, NerveETN684
- Shunt, Central Nervous System And ComponentsJXG627
- Catheter, Continuous FlushKRA239
- Electrode, NeedleGXZ95
- Bur, Ear, Nose And ThroatEQJ88
- Port & Catheter, Implanted, Subcutaneous, IntraventricularLKG19
- Catheter, Percutaneous, Intraspinal, Short TermMAJ16
- Neurological Stereotaxic InstrumentHAW5
- Replacement, Ossicular Prosthesis, TotalETA3
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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