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
- 1,721
- Deaths
- 15
- Injuries
- 318
- Malfunctions
- 1,388
Reports per year
120
422
1123
45824
88925
35826
Source: FDA adverse event reports by year received, 2020–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stimulator, NerveETN657
- Shunt, Central Nervous System And ComponentsJXG613
- Catheter, Continuous FlushKRA228
- Electrode, NeedleGXZ94
- Bur, Ear, Nose And ThroatEQJ87
- Port & Catheter, Implanted, Subcutaneous, IntraventricularLKG15
- Catheter, Percutaneous, Intraspinal, Short TermMAJ15
- 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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