Stryker Neurovascular-utah-salt Lake City
FDA adverse event reports naming Stryker Neurovascular-utah-salt Lake City as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY.
- Total reports
- 1,630
- Deaths
- 27
- Injuries
- 556
- Malfunctions
- 1,047
Reports per year
4218
11419
22520
21821
23522
26723
22324
20325
10326
Source: FDA adverse event reports by year received, 2018–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Wire, Guide, CatheterDQX781
- Guide, Wire, Catheter, NeurovasculatureMOF347
- Catheter, Thrombus RetrieverNRY207
- Catheter, PercutaneousDQY179
- Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke TreatmentPOL83
- Catheter, Intravascular, DiagnosticDQO23
- Catheter, Percutaneous, NeurovasculatureQJP8
- Intracranial Aneurysm Flow DiverterOUT2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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