Boston Scientific - Galway
FDA adverse event reports naming Boston Scientific - Galway as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BOSTON SCIENTIFIC - GALWAY.
- Total reports
- 37,538
- Deaths
- 1,891
- Injuries
- 12,652
- Malfunctions
- 22,975
Reports per year
306
1809
2,84410
2,53511
3,83012
4,33913
3,65714
4,32915
6,13816
6,10617
3,73918
Source: FDA adverse event reports by year received, 2006–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Coronary Drug-Eluting StentNIQ23,638
- Stents, Drains And Dilators For The Biliary DuctsFGE3,921
- Catheter, Angioplasty, Peripheral, TransluminalLIT1,741
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX1,333
- Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/ScoringNWX1,095
- System, Appendage Closure, Left AtrialNGV1,017
- Prosthesis, EsophagealESW983
- Stent, CoronaryMAF751
- Prosthesis, Tracheal, ExpandableJCT631
- Stent, Colonic, Metallic, ExpandableMQR474
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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