Boston Scientific Ireland Ltd.
FDA adverse event reports naming Boston Scientific Ireland Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BOSTON SCIENTIFIC IRELAND LTD..
- Total reports
- 1,687
- Deaths
- 174
- Injuries
- 565
- Malfunctions
- 948
Reports per year
104
106
1108
1,04709
62710
Source: FDA adverse event reports by year received, 2004–2010. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Coronary Drug-Eluting StentNIQ820
- Stent, CoronaryMAF459
- Stent, CarotidNIM89
- Stents, Drains And Dilators For The Biliary DuctsFGE79
- Prosthesis, Tracheal, ExpandableJCT40
- Dilator, Catheter, UreteralEZN38
- Stent, Colonic, Metallic, ExpandableMQR33
- Prosthesis, EsophagealESW31
- Catheter, Angioplasty, Peripheral, TransluminalLIT28
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX24
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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