Stryker Neurovascular Cork
FDA adverse event reports naming Stryker Neurovascular Cork as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER NEUROVASCULAR CORK.
- Total reports
- 6,685
- Deaths
- 157
- Injuries
- 2,415
- Malfunctions
- 4,113
Reports per year
112
27413
23914
23515
43116
53517
55018
41819
41120
54921
65822
59723
62424
74825
41526
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Device, Neurovascular EmbolizationHCG2,741
- Intracranial Neurovascular StentNJE1,339
- Intracranial Aneurysm Flow DiverterOUT939
- Catheter, PercutaneousDQY712
- Intracranial Coil-Assist StentQCA444
- Catheter, Intravascular Occluding, TemporaryMJN377
- Catheter, Thrombus RetrieverNRY99
- Catheter, Continuous FlushKRA13
- Pump, Portable, Aspiration (Manual Or Powered)BTA4
- Catheter, Percutaneous, NeurovasculatureQJP4
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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