Medtronic Cardiovascular Santa Rosa
FDA adverse event reports naming Medtronic Cardiovascular Santa Rosa as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC CARDIOVASCULAR SANTA ROSA.
- Total reports
- 2,265
- Deaths
- 307
- Injuries
- 1,724
- Malfunctions
- 234
Reports per year
21711
57412
25613
22814
31215
20416
9817
11918
4119
3620
3221
3322
823
1424
725
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Endovascular Graft, Aortic Aneurysm TreatmentMIH2,088
- Endovascular Suturing SystemOTD93
- Stent, IliacNIO29
- Coronary Drug-Eluting StentNIQ24
- Introducer, CatheterDYB14
- Stent, CoronaryMAF5
- Stents, Drains And Dilators For The Biliary DuctsFGE4
- Catheter, PercutaneousDQY3
- Stent, Superficial Femoral ArteryNIP3
- Wire, Guide, CatheterDQX2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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