Boston Scientific - Cork
FDA adverse event reports naming Boston Scientific - Cork as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BOSTON SCIENTIFIC - CORK.
- Total reports
- 6,978
- Deaths
- 250
- Injuries
- 1,940
- Malfunctions
- 4,786
Reports per year
109
1,00010
84611
81112
64813
64814
82415
76516
87717
55818
Source: FDA adverse event reports by year received, 2009–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Coronary, AtherectomyMCX1,763
- Device, Vascular, For Promoting EmbolizationKRD860
- Syringe, Balloon InflationMAV822
- Device, Neurovascular EmbolizationHCG710
- Stents, Drains And Dilators For The Biliary DuctsFGE587
- Catheter, Continuous FlushKRA481
- Dilator, EsophagealKNQ388
- Catheter, Peripheral, AtherectomyMCW265
- Catheter, PercutaneousDQY261
- Bronchial Thermoplasty SystemOOY224
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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