Medtronic Cardiovascular Galway
FDA adverse event reports naming Medtronic Cardiovascular Galway as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC CARDIOVASCULAR GALWAY.
- Total reports
- 3,839
- Deaths
- 591
- Injuries
- 2,372
- Malfunctions
- 871
Reports per year
55508
82109
1,79910
65911
214
315
Source: FDA adverse event reports by year received, 2008–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Coronary Drug-Eluting StentNIQ2,233
- System, Endovascular Graft, Aortic Aneurysm TreatmentMIH1,085
- Stent, CoronaryMAF287
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX195
- Catheter, PercutaneousDQY22
- Stents, Drains And Dilators For The Biliary DuctsFGE9
- Stent, IliacNIO6
- Product code ------1
- Wire, Guide, CatheterDQX1
- 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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