Boston Scientific - Maple Grove
FDA adverse event reports naming Boston Scientific - Maple Grove as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BOSTON SCIENTIFIC - MAPLE GROVE.
- Total reports
- 26,805
- Deaths
- 1,025
- Injuries
- 7,952
- Malfunctions
- 17,821
Reports per year
204
305
406
609
1,98110
2,82611
3,40612
2,91413
2,54514
2,86315
4,08916
3,98917
2,17718
Source: FDA adverse event reports by year received, 2004–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheters, Transluminal Coronary Angioplasty, PercutaneousLOX7,805
- Coronary Drug-Eluting StentNIQ5,374
- Catheter, PercutaneousDQY3,342
- Catheter, Angioplasty, Peripheral, TransluminalLIT2,930
- System, Appendage Closure, Left AtrialNGV1,523
- Stent, CoronaryMAF1,449
- Catheter, EmbolectomyDXE929
- Wire, Guide, CatheterDQX607
- Stent, Superficial Femoral ArteryNIP548
- Stents, Drains And Dilators For The Biliary DuctsFGE528
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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